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Dicyclohexylchlorophosphine

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Dicyclohexylchlorophosphine Basic information
Product Name:Dicyclohexylchlorophosphine
Synonyms:Chlorodicyclohexylphosphine ,96%;Chlorodicyclohexylphosphine, 97% 5GR;98% (C6H11)2PCl;Phosphinous chloride, P,P-dicyclohexyl-;Chlorodicyclohexylphosphine 97%;Chlorodicyclohexylphosphine Synonyms Dicyclohexylchlorophosphine;Dicyclohexylphosphine chloride;DICYCLOHEXYLPHOSPHINOUS CHLORIDE
CAS:16523-54-9
MF:C12H22ClP
MW:232.73
EINECS:
Product Categories:organophosphine halide;Achiral Phosphine;Alkyl Phosphine;P-Cl;Catalysis and Inorganic Chemistry;Phosphorus Compounds;Phosphorus Precursors;Chlorophosphines;Phosphines
Mol File:16523-54-9.mol
Dicyclohexylchlorophosphine Structure
Dicyclohexylchlorophosphine Chemical Properties
Melting point 126-128 °C
Boiling point 165 °C/12 mmHg (lit.)
density 1.054 g/mL at 25 °C (lit.)
refractive index n20/D 1.533(lit.)
Fp >230 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form Liquid
Specific Gravity1.054
color Colorless to pale yellow
Water Solubility reacts violently
Sensitive Air & Moisture Sensitive
InChIInChI=1S/C12H22ClP/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-12H,1-10H2
InChIKeyAKJFBIZAEPTXIL-UHFFFAOYSA-N
SMILESP(C1CCCCC1)(C1CCCCC1)Cl
CAS DataBase Reference16523-54-9(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 14-34
Safety Statements 26-27-36/37/39-45-8
RIDADR UN 3265 8/PG 2
WGK Germany 3
TSCA No
HazardClass 8
PackingGroup II
HS Code 29319090
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsEye Dam. 1
Skin Corr. 1B
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Dicyclohexylchlorophosphine Usage And Synthesis
Chemical Propertiesclear colorless liquid
UsesDicyclohexylchlorophosphine is used as pharmaceutical intermediate. It is also used in the synthesis of various phosphines.
UsesChlorodicyclohexylphosphine can be used as a reactant in the synthesis of:
  • 1,2-Bis(dicyclohexylphosphinoxy)ethane ligand by reacting with ethylene glycol in the presence of triethylamine via MichaelisArbuzov type rearrangements.
  • 1,1,2,2-tetracyclohexyldiphosphine monosulfide ligand by treating with LiS.

It can be also used as a starting material for the preparation of some other ligands such as dicyclohexylphosphine oxide , phosphino substituted N-aryl pyrroles , di-tert-butyl((dicyclohexylphosphino)methyl)phosphine , dicyclohexylcyclopentylphosphine. These ligands are used in Pd-catalyzed cross-coupling reactions.
ApplicationChlorodicyclohexylphosphine can be used as a reactant in the synthesis of:
1,2-Bis(dicyclohexylphosphinoxy)ethane ligand by reacting with ethylene glycol in the presence of triethylamine via MichaelisArbuzov type rearrangements.
1,1,2,2-tetracyclohexyldiphosphine monosulfide ligand by treating with LiS.
It can be also used as a starting material for the preparation of some other ligands such as dicyclohexylphosphine oxide , phosphino substituted N-aryl pyrroles , di-tert-butyl((dicyclohexylphosphino)methyl)phosphine , dicyclohexylcyclopentylphosphine. These ligands are used in Pd-catalyzed cross-coupling reactions.
reaction suitabilityreaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
SynthesisDicyclohexylphosphine (98.8%,10.68 g,53.8 mmol) was added to the reaction flask followed by THF (10.85 g). Ethyl trichloroacetate (97%,10.52g,55mmol) was added dropwise to the resulting solution over a period of 30 minutes under stirring (the temperature of the reaction mixture was varied from 18C to 33C by applying external cooling during the addition). The reaction mixture was aged at ambient temperature for two hours (aging means keeping the reaction mixture under specified conditions for a specified time, optionally under stirring). After aging, the reaction mixture was a clear and colorless low viscosity liquid. The crude reaction mixture was subjected to vacuum distillation (96-100 C/3.6 mbar), which resulted in the isolation of dicyclohexylphosphonium chloride in 53% yield and high purity as a clear and colorless low-viscous liquid (31P NMR: 98.78% ;GC-FID: 97.26%).
PrecautionsStore in cool, dry conditions in well sealed containers. Protect from humidity and water. Store under dry inert gas. It is sensitive to air and moisture. Incompatible with strong oxidizing agents.
Tag:Dicyclohexylchlorophosphine(16523-54-9) Related Product Information
Trimethylamine hydrochloride Tetramethylammonium chloride Tricyclohexyl phosphine Benzyltriethylammonium chloride Benzyltrimethylammonium chloride Didecyl dimethyl ammonium chloride Isopropylmagnesium chloride Tris(triphenylphosphine)chlororhodium Dicyclohexylcarbodiimide Dicyclohexylphenylphosphine Tungstic acid DICYCLOHEXYLPHOSPHINE Cyclohexylphosphine Dicyclohexylphosphinyl chloride Dichloro(chlorodicyclohexylphosphine) palladium (II) dimer Dichlorobis(chlorodicyclohexylphosphine) palladium (II) Di-1-adamantylphosphinic chloride Dicyclohexylchlorophosphine