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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896891Generated: October 29, 2026

Benzenesulfonyl chloride → HCID 689074, compound

https://huagongshe.com/reaction/896891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant4-Bromophenacyl bromideHCID 7454—
CatalystZincHCID 23994—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 689074HCID 689074—

Reaction Steps

To benzenesulfonyl chloride (0.5 mL, 3.92 mmol) in 4:1 v/v tetrahydrofuran—water (20 mL) was added powdered zinc (282 mg, 4.31 mmol, 1.1 eq.) followed by 4-bromophenacyl bromide (1.31 g, 4.70 mmol, 1.2 eq.). The reaction mixture was stirred at room temperature for 17 hours. The volatile solvent was evaporated under reduced pressure and poured into water. The reaction was extracted with ethyl acetate (2×150 mL), and the combined organic layers were washed with brine (1×100 mL), dried (MgSO4), filtered, and evaporated under reduce pressure. The crude product was purified using MPLC (Biotage) eluted with 5:1 v/v hexane-ethyl acetate. Crystallization from dichloromethane-hexane gave the desired product as a white fluffy solid (486 mg, 36.6% yield). MS LC-MS (ES MH+=340); TLC (Rf=0.30, 25% ethyl acetate-hexane)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919371B2
Source datasetuspto-grants-2005_07
ORD IDord-058adeb4ff214bfc932bbb1c3e6f82e3
Source noteuspto-grants-2005_07