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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703350Generated: October 30, 2026

Chloride → HCID 14403425, compound

https://huagongshe.com/reaction/703350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantHCID 53893725HCID 53893725—
ReactantHCID 178418361HCID 178418361—
SolventTolueneHCID 1140—
ProductHCID 14403425HCID 1440342590%

Reaction Conditions

Temperature50 °C

Reaction Steps

460 mg (0.5 mmol) of tris-triphenylphosphinerhodium chloride (=1 mol-%, with respect to the reaction component) are added to a 100 ml autoclave. After purging with nitrogen, an air-free solution of 15.7 g (0.05 mol) of 4-chlorophenyl-ethenyl 1-phenylmercapto-cyclopropyl ketone in 40 ml of toluene is added and the mixture is heated to 50° C. under a hydrogen pressure of 30 bar. The hydrogen pressure is held between 40 and 50 bar until gas uptake has ended. The mixture is then reacted for a further hour. For working up, the solvent is stripped off under reduced pressure and the residue remaining is purified on silica gel using dichloromethane as eluant. 14.2 g (90% of theory) of 4-chlorophenylethyl 1-phenylmercaptocyclopropyl ketone are obtained in the form of an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983208
Source datasetuspto-grants-1991_01
ORD IDord-d5fa91bcbdd94144abddbb294a12b0a2
Source noteuspto-grants-1991_01