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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3079Generated: October 28, 2026

Thionyl Chloride → 1-Hydroxycyclohexyl 4-(2-chloroformylethyl)carbonylphenyl ketone

https://huagongshe.com/reaction/3079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-Hydroxycyclohexyl 4-(2-carboxyethyl)carbonylphenyl ketoneHCID 18323517—
SolventDiethyl EtherHCID 3283—
Product1-Hydroxycyclohexyl 4-(2-chloroformylethyl)carbonylphenyl ketoneHCID 5396471394%

Reaction Conditions

Temperature30 °C

Reaction Steps

A 250-ml round-bottomed flask fitted with a condenser was charged with 12.0 g of 1-hydroxycyclohexyl 4-(2-carboxyethyl)carbonylphenyl ketone (0.04 mole), 5.95 g (0.05 mole) of thionyl chloride (Aldrich), and 50 ml of diethyl ether. The resulting reaction mixture was stirred at 30° C. for 30 minutes, after which time the solvent was removed under reduced pressure. The residue, a white solid, was maintained at 0.01 Torr =30 minutes to remove residual solvent and excess thionyl chloride, leaving 12.1 g (94 percent) of 1-hydroxycyclohexyl 4-(2-chloroformylethyl)carbonylphenyl ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733693
Source datasetuspto-grants-1998_03
ORD IDord-2d4f64dd7b0a4a1ab9ebcd6c62f6820c
Source noteuspto-grants-1998_03