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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21460Generated: October 30, 2026

Triphenylphosphine → 2-Chloro-4-(methylsulfanyl)benzaldehyde

https://huagongshe.com/reaction/21460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Chloro-4-methylsulphenylbenzoyl chlorideHCID 18977956—
CatalystBis (triphenylphosphine) copper (I) borohydrideHCID 10908163—
SolventAcetoneHCID 180—
Product2-Chloro-4-(methylsulfanyl)benzaldehydeHCID 1993179098.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 2-chloro-4-(methylsulphenyl)-benzoyl chloride (1.0 g), triphenyl phosphine (2.47 g) and bis(triphenylphosphine)copper (I) borohydride (1.0 g) in acetone was stirred at 0° C. for 1 hour. Further his (triphenylphosphine)copper (I) borohydride (1.5 g) was added and the mixture was stirred for 2 hours. The mixture was filtered and the filtrate was evaporated to dryness. The residue was dissolved in chloroform and treated with copper (I) bromide (2.1 g). The filtrate was evaporated to dryness and the residue was purified by chromotography eluted with a mixture of ethyl acetate and hexane to give 2-chloro-4-(methylsulphenyl)benzaldehyde (0.83 g) as an off-white solid, m.p. 76°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424276
Source datasetuspto-grants-1995_06
ORD IDord-2216a806563e452ca7db02216554b46a
Source noteuspto-grants-1995_06