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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957939Generated: October 30, 2026

Ethyl phenylacetate → (4-Chlorosulfonyl-phenyl)-acetic acid ethyl ester

https://huagongshe.com/reaction/1957939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl phenylacetateHCID 7590—
ReactantChlorosulfonic acidHCID 24638—
Product(4-Chlorosulfonyl-phenyl)-acetic acid ethyl esterHCID 1046790056.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

The chlorosulfonic acid (16.6 mL, 250 mmol) was added dropwise into ethyl phenylacetate (8.2 g, 50 mmol) under stirring at 40° C. Thereafter, the mixture was stirred for 0.5 hour at room temperature, and then poured on ice and extracted with dichloromethane. The combined organic phase was washed by saline, dried with sodium sulfate and concentrated under reduced pressure. The concentrate was separated through column chromatography (petroleum ether/ethyl acetate=6/1, v/v) to obtain yellow oil (7.4 g, yield: 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410094B2
Source datasetuspto-grants-2013_04
ORD IDord-9bd4a204d30d43f1acb4bd26ce5b8560
Source noteuspto-grants-2013_04