Misplaced Pages

Triphenylphosphine dichloride: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 12:26, 20 May 2011 editCitation bot (talk | contribs)Bots5,391,530 editsm +: issue.← Previous edit Latest revision as of 00:41, 8 June 2023 edit undoPlantman (talk | contribs)Extended confirmed users811 edits // Edit via WikiplusTags: Mobile edit Mobile web edit Advanced mobile edit 
(24 intermediate revisions by 17 users not shown)
Line 1: Line 1:
{{chembox {{chembox
| Verifiedfields = changed
⚫ | verifiedrevid = 360130922
| Watchedfields = changed
⚫ | Name = Triphenylphosphine dichloride
⚫ | verifiedrevid = 430032953
⚫ | ImageFile = Dichlorotriphenylphosphine-2D.png
⚫ | Name = Triphenylphosphine dichloride
⚫ | ImageSize = 150px
⚫ | ImageFile = Dichlorotriphenylphosphine-2D.png
⚫ | ImageName = Structural formula
⚫ | ImageSize = 150px
⚫ | ImageFileL1 = Dichlorotriphenylphosphine-molecular-from-xtal-1998-3D-balls.png
⚫ | ImageName = Structural formula
| ImageSizeL1 = 150px
⚫ | ImageFileL1 = Dichlorotriphenylphosphine-molecular-from-xtal-1998-3D-balls.png
| ImageNameL1 = Ball-and-stick model | ImageNameL1 = Ball-and-stick model
| ImageFileR1 = Dichlorotriphenylphosphine-molecular-from-xtal-1998-3D-vdW.png | ImageFileR1 = Dichlorotriphenylphosphine-molecular-from-xtal-1998-3D-vdW.png
| ImageSizeR1 = 150px
| ImageNameR1 = Space-filling model | ImageNameR1 = Space-filling model
| IUPACName = Dichlorotriphenyl-λ<sup>5</sup>-phosphane | PIN = Dichlorotri(phenyl)-λ<sup>5</sup>-phosphane
| OtherNames =Dichlorotriphenylphosphorane | OtherNames =Dichlorotriphenylphosphorane
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo = 2526-64-9 | CASNo = 2526-64-9
| CASNo_Ref = {{cascite|correct|CAS}}
| RTECS =
| UNII_Ref = {{fdacite|correct|FDA}}
⚫ }}

⚫ | Section2 = {{Chembox Properties
| UNII = 6CL2293LZ3
⚫ | Formula = C<sub>18</sub>H<sub>15</sub>Cl<sub>2</sub>P
| PubChem = 260420
⚫ | MolarMass = 333.19 g/mol
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| Appearance =
| Density = | ChemSpiderID = 228579
| SMILES = ClP(Cl)(c1ccccc1)(c1ccccc1)c1ccccc1
⚫ | Solubility =
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
⚫ | MeltingPt = 176 °C<ref name="Grignard">{{ cite journal | author = ], J. Savard | journal = ] | year = 1931 | volume = 192 | pages = 592–5 }}</ref>, 85-100 °C<ref name="e-EROS">], {{doi|10.1002/047084289X.rt371}}</ref>
| StdInChI = 1S/C18H15Cl2P/c19-21(20,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
| BoilingPt =
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| RefractIndex =
| StdInChIKey = ASWXNYNXAOQCCD-UHFFFAOYSA-N
⚫ }}
⚫ }}
| Section3 = {{Chembox Structure
⚫ |Section2={{Chembox Properties
| MolShape =
⚫ | Formula = C<sub>18</sub>H<sub>15</sub>Cl<sub>2</sub>P
| Dipole =
⚫ | MolarMass = 333.19 g/mol
⚫ }}
⚫ | Solubility = Reacts
| Section7 = {{Chembox Hazards
| ExternalMSDS = | MeltingPtC = 176
⚫ | MeltingPt_ref = <ref name="Grignard">{{cite journal | author = ], J. Savard | journal = ] | year = 1931 | volume = 192 | pages = 592–5}}</ref> 85-100 °C<ref name="e-EROS">], {{doi|10.1002/047084289X.rt371}}</ref>
| EUClass =
⚫ }}
| FlashPt =
⚫ |Section8={{Chembox Related
| RPhrases =
⚫ | OtherCompounds = ]s<br/>]<br/>]<br/>]<br/>]<br/>]
| SPhrases =
⚫ }}
| RSPhrases =
}}
⚫ | Section8 = {{Chembox Related
| Function =
| OtherFunctn =
⚫ | OtherCpds = ]s<br/>]<br/>]<br/>]<br/>]<br/>]
}}
}} }}


'''Triphenylphosphine dichloride''', Ph<sub>3</sub>PCl<sub>2</sub>, is a ] widely used in organic chemistry. Applications include the conversion of ]s and ]s to ]s, the cleavage of ]s to vicinal dichlorides and the chlorination of ]s to ]s.<ref name="e-EROS" /> '''Triphenylphosphine dichloride''', (C<sub>6</sub>H<sub>5</sub>)<sub>3</sub>PCl<sub>2</sub>, is a ] widely used in organic chemistry. Applications include the conversion of ]s and ]s to ]s, the cleavage of ]s to vicinal dichlorides and the chlorination of ]s to ]s.<ref name="e-EROS" />


== Structure == == Structure ==
In ] solvents such as ] or ] solutions, Ph<sub>3</sub>PCl<sub>2</sub> adopts an ionic ] structure, Cl<sup>&minus;</sup>,<ref name="Godfrey 1996">{{ cite journal | journal = ] | year = 1996 | pages = 2521−2522 | doi = 10.1039/CC9960002521 | author = S. M. Godfrey, C. A. McAuliffe, R. G. Pritchard, J. M. Sheffield | title = An X-ray crystallorgraphic study of the reagent Ph3PCl2; not charge-transfer, R3P–Cl–Cl, trigonal bipyramidal or Cl but an unusual dinuclear ionic species, Cl containing long Cl–Cl contacts | issue = 22 }}</ref> whereas in non-polar solvents like ] it exists as a non-solvated ] molecule.<ref name="Godfrey 1998">{{ cite journal | journal = Chem. Commun. | year = 1998 | pages = 921−922 | doi = 10.1039/a800820e | author = S. M. Godfrey, C. A. McAuliffe, J. M. Sheffield | title = Structural dependence of the reagent Ph3PCl2 on the nature of the solvent, both in the solid state and in solution; X-ray crystal structure of trigonal bipyramidal Ph3PCl2, the first structurally characterised five-coordinate R3PCl2 compound | issue = 8 }}</ref> Two species can also adopt an unusual dinuclear ionic structure&mdash;both interacting with a Cl<sup>&minus;</sup> via long Cl&ndash;Cl contacts.<ref name="Godfrey 1996"/> In ]s such as ], Ph<sub>3</sub>PCl<sub>2</sub> adopts an ionic ] structure, Cl<sup>&minus;</sup>,<ref name="Godfrey 1996">{{cite journal | journal = ] | year = 1996 | pages = 2521–2522 | doi = 10.1039/CC9960002521 |author1=S. M. Godfrey |author2=C. A. McAuliffe |author3=R. G. Pritchard |author4=J. M. Sheffield | title = An X-ray crystallorgraphic study of the reagent Ph3PCl2; not charge-transfer, R3P–Cl–Cl, trigonal bipyramidal or Cl but an unusual dinuclear ionic species, Cl containing long Cl–Cl contacts | issue = 22}}</ref> whereas in non-polar solvents like ] it exists as a non-solvated ] molecule.<ref>{{cite journal | journal = Chem. Commun. | year = 1998 | pages = 921–922 | doi = 10.1039/a800820e |author1=S. M. Godfrey |author2=C. A. McAuliffe |author3=J. M. Sheffield | title = Structural dependence of the reagent Ph3PCl2 on the nature of the solvent, both in the solid state and in solution; X-ray crystal structure of trigonal bipyramidal Ph3PCl2, the first structurally characterised five-coordinate R3PCl2 compound | issue = 8}}</ref> Two species can also adopt an unusual dinuclear ionic structure&mdash;both interacting with a Cl<sup>&minus;</sup> via long Cl–Cl contacts.<ref name="Godfrey 1996"/>


<gallery> <gallery>
Line 63: Line 57:


Both reagents are typically used in solution to ensure the correct ].<ref name="e-EROS" /> Both reagents are typically used in solution to ensure the correct ].<ref name="e-EROS" />

Ph<sub>3</sub>PCl<sub>2</sub> can also be obtained by the reaction of iodobenzene dichloride (PhICl<sub>2</sub>) and triphenylphosphine.<ref>Carle, M. S., Shimokura, G. K. and Murphy, G. K. (2016), Iodobenzene Dichloride in the Esterification and Amidation of Carboxylic Acids: In-Situ Synthesis of Ph3PCl2. ], 2016: 3930–3933. {{DOI:10.1002/ejoc.201600714}}</ref>


Alternatively, Ph<sub>3</sub>PCl<sub>2</sub> can be obtained by chlorination of ] with, for example, ], as in Grignard's original 1931 synthesis.<ref name="Grignard" /> Alternatively, Ph<sub>3</sub>PCl<sub>2</sub> can be obtained by chlorination of ] with, for example, ], as in Grignard's original 1931 synthesis.<ref name="Grignard" />
Line 70: Line 66:


] ]
]
]

Latest revision as of 00:41, 8 June 2023

Triphenylphosphine dichloride
Structural formula
Ball-and-stick model
Ball-and-stick model
Space-filling model
Space-filling model
Names
Preferred IUPAC name Dichlorotri(phenyl)-λ-phosphane
Other names Dichlorotriphenylphosphorane
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.107.819 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C18H15Cl2P/c19-21(20,16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15HKey: ASWXNYNXAOQCCD-UHFFFAOYSA-N
SMILES
  • ClP(Cl)(c1ccccc1)(c1ccccc1)c1ccccc1
Properties
Chemical formula C18H15Cl2P
Molar mass 333.19 g/mol
Melting point 176 °C (349 °F; 449 K) 85-100 °C
Solubility in water Reacts
Related compounds
Related compounds Phosphoranes
Triphenylphosphine
Phosphorus trichloride
Phosphorus pentachloride
Phosphorus halides
Tetraphenylphosphonium chloride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Triphenylphosphine dichloride, (C6H5)3PCl2, is a chlorinating agent widely used in organic chemistry. Applications include the conversion of alcohols and ethers to alkyl chlorides, the cleavage of epoxides to vicinal dichlorides and the chlorination of carboxylic acids to acyl chlorides.

Structure

In polar solvents such as acetonitrile, Ph3PCl2 adopts an ionic phosphonium salt structure, Cl, whereas in non-polar solvents like diethyl ether it exists as a non-solvated trigonal bipyramidal molecule. Two species can also adopt an unusual dinuclear ionic structure—both interacting with a Cl via long Cl–Cl contacts.

Synthesis

Triphenylphosphine dichloride is usually prepared fresh by the addition of chlorine to triphenylphosphine.

Ph3P + Cl2 → Ph3PCl2

Both reagents are typically used in solution to ensure the correct stoichiometry.

Ph3PCl2 can also be obtained by the reaction of iodobenzene dichloride (PhICl2) and triphenylphosphine.

Alternatively, Ph3PCl2 can be obtained by chlorination of triphenylphosphine oxide with, for example, phosphorus trichloride, as in Grignard's original 1931 synthesis.

References

  1. ^ Victor Grignard, J. Savard (1931). Comptes rendus de l'Académie des sciences. 192: 592–5. {{cite journal}}: Missing or empty |title= (help)
  2. ^ e-EROS Encyclopedia of Reagents for Organic Synthesis, doi:10.1002/047084289X.rt371
  3. ^ S. M. Godfrey; C. A. McAuliffe; R. G. Pritchard; J. M. Sheffield (1996). "An X-ray crystallorgraphic study of the reagent Ph3PCl2; not charge-transfer, R3P–Cl–Cl, trigonal bipyramidal or Cl but an unusual dinuclear ionic species, Cl containing long Cl–Cl contacts". Chemical Communications (22): 2521–2522. doi:10.1039/CC9960002521.
  4. S. M. Godfrey; C. A. McAuliffe; J. M. Sheffield (1998). "Structural dependence of the reagent Ph3PCl2 on the nature of the solvent, both in the solid state and in solution; X-ray crystal structure of trigonal bipyramidal Ph3PCl2, the first structurally characterised five-coordinate R3PCl2 compound". Chem. Commun. (8): 921–922. doi:10.1039/a800820e.
  5. Carle, M. S., Shimokura, G. K. and Murphy, G. K. (2016), Iodobenzene Dichloride in the Esterification and Amidation of Carboxylic Acids: In-Situ Synthesis of Ph3PCl2. Eur. J. Org. Chem., 2016: 3930–3933. {{DOI:10.1002/ejoc.201600714}}
Categories: