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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649631Generated: November 2, 2026

Chlorosulfonic acid → HCID 19854187, compound

https://huagongshe.com/reaction/1649631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantHCID 19854198HCID 19854198—
SolventChloroformHCID 6212—
ProductHCID 19854187HCID 19854187—

Reaction Steps

Chlorosulphonic acid (20 ml) was added dropwise to an ice-cold solution of 3-hydroxy-2-propionyl-4-(4-methylphenyl)cyclohex-2-ene-1-one (3.25 g) in chloroform (40 ml). After stirring at room temperature for 4 hours, the mixture was carefully poured onto ice. The chloroform layer was separated and the aqueous phase extracted with more chloroform. The combined extracts were dried over magnesium sulphate, filtered and the chloroform evaporated in vacuo to give 3-hydroxy-2-propionyl-4-(3-chlorosulphonyl-4-methylphenyl)cyclohex-2-ene-1-one (4.4 g). Water (50 ml) was added to the latter, followed by dimethylamine (2 g) and the solution stirred at room temperature for 1/2 hour. The solution was acidified with dilute hydrochloric acid, and extracted with dichloromethane. After drying over magnesium sulphate, the dichloromethane was evaporated in vacuo to give a pale yellow oil. Purification on a silica gel column using chloroform as eluant gave the title compound (4.0 g) as a white solid of m.p. 95°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921524
Source datasetuspto-grants-1990_05
ORD IDord-80ae5a4a181f4706ab5ceb2954de84a6
Source noteuspto-grants-1990_05