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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35764Generated: October 25, 2026

Chlorosulfonic acid → HCID 178458849, compound

https://huagongshe.com/reaction/35764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 178458835HCID 178458835—
SolventChloroformHCID 6212—
ProductHCID 178458849HCID 178458849—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 3-hydroxy-5-mesityl-2-propionylcyclohex-2-en-1-one (1.8 g) in chloroform (20 ml) was stirred and cooled to 0° C. during the dropwise addition of chlorosulphonic acid (10 ml). The mixture was stirred for four hours at 20° C. and then poured into ice-water and the aqueous phase was extracted with chloroform (50 ml). The organic phase was dried over anhydrous sodium sulphate and the solvent was removed by evaporation under reduced pressure using a rotary evaporator. The product 3-hydroxy-5-(2,4,6-trimethyl-3-chlorosulphonylphenyl)-2-propionylcyclohex-2-en-1-one was isolated as a brown oil (2.4 g, 97%). Proton magnetic resonance spectrum (CDCl3 ; δ in ppm): 1.16 (3H, t); 2.47 (3H, s); 2.69 (3H, s); 2.80 (3H, s); 2.7-4.0 (7H, m); 7.05 (1H, s); 18.30 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767879
Source datasetuspto-grants-1988_08
ORD IDord-f1f47e8355734a17843cc0977077ff83
Source noteuspto-grants-1988_08