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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209669Generated: October 30, 2026

Dihydrobenzofuran → 2,3-Dihydrobenzofuran-5-sulfonyl Chloride

https://huagongshe.com/reaction/2209669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDihydrobenzofuranHCID 10329—
ReactantChlorosulfonic acidHCID 24638—
Product2,3-Dihydrobenzofuran-5-sulfonyl ChlorideHCID 277615430.2%

Reaction Steps

2,3-dihydrobenzofuran (6.0 g, 49.94 mmol) is added over 20 minutes to chlorosulfonic acid (29.09 g, 249.69 mmol) at -20° C. The reaction mixture is quenched by addition of ice followed by water (20 mL). The mixture is then extracted with ethyl acetate. The combined organic estracts are washed with brine, dried (Na2SO4), and the solvent is evaporated. The crude product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give 2,3-dihydrobenzofuran-5-sulfonyl chloride (3.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-cb8419eb67094748a96a0fd327e9a9a8
Source noteuspto-grants-1995_10