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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749497Generated: November 2, 2026

Chlorosulfonic acid → p-(2-Acetamidoethyl)benzenesulphonyl chloride

https://huagongshe.com/reaction/1749497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantN-(2-phenylethyl)acetamideHCID 70143—
Productp-(2-Acetamidoethyl)benzenesulphonyl chlorideHCID 301578245%

Reaction Steps

N-Phenethylacetamide (4.50 g, 27.6 mmol) was added to sulfurochloridic acid (30 mL) slowly at 0-5° C. The resulting reaction mixture was stirred at room temperature for 2 h. The reaction mixture was poured into ice-water and stirred for 10 min. The mixture was extracted with DCM. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated to afford the title compound as a brown solid (3.30 g, 12.64 mmol, 45% yield). MS (ESI) m/z 262.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156798B2
Source datasetuspto-grants-2015_10
ORD IDord-3f24ffb28f2141bbb946d7b287d56a41
Source noteuspto-grants-2015_10