Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4761Generated: October 26, 2026

1,3-Dichloropropane → Phosphine, (3-chloropropyl)diphenyl-

https://huagongshe.com/reaction/4761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloropropaneHCID 8881—
ReactantDiphenylphosphineHCID 70017—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418495HCID 178418495—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductPhosphine, (3-chloropropyl)diphenyl-HCID 608029—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 500 mL round bottom flask there was added 400 mL of dry tetrahydrofuran followed by 0.081 mole of HPPh2. The mixture was cooled to 0° C. and 0.081 mole of n-butyl lithium was slowly added to generate LiPPh2 ; this was slowly warmed to room temperature and stirred for about one hour. The solution was transferred to a dropping funnel and added dropwise to a flask containing 100 mL of 1,3-dichloropropane dissolved in 100 mL of diethyl ether. After stirring overnight the mixture was hydrolyzed with 25 mL of water. The organic layer was separated and the solvent removed by vacuum to leave Ph2P(CH2)3Cl that was stored under nitrogen until needed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04727200
Source datasetuspto-grants-1988_02
ORD IDord-12421d0797394bc59f5eb474f7a37fd6
Source noteuspto-grants-1988_02