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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927970Generated: October 27, 2026

Chlorosulfonic acid → HCID 86713311, compound

https://huagongshe.com/reaction/927970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
ReactantMethyl 3-fluorophenylacetateHCID 2734108—
ProductHCID 86713311HCID 86713311—

Reaction Steps

Methyl (3-fluorophenyl)acetate (1.51 g) was added dropwise to chlorosulphonic acid (7 mL) with stirring and ice cooling. The cooling bath was removed and the mixture was allowed to stand at room temperature for 16 hours before being carefully added to a mixture of ice and ethyl acetate. The organic layer was separated, washed with water, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-20% to give methyl (2-chlorosulfonyl-5-fluorophenyl)acetate (1.42 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-9c6cece0184b46298d44fb4f245e6fee
Source noteuspto-grants-2016_03