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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256062Generated: October 26, 2026

N-(3-Fluorophenyl)acetamide → 4-Acetamido-2-fluorobenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1256062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Fluorophenyl)acetamideHCID 9594—
ReactantChlorosulfonic acidHCID 24638—
Product4-Acetamido-2-fluorobenzene-1-sulfonyl chlorideHCID 1677108418%

Reaction Conditions

Temperature0 °C

Reaction Steps

Neat N-(3-fluorophenyl)acetamide (5 g, 32.65 mmol) was put on an ice-water bath and had chlorosulfonic acid added drop-wise. The solution was stirred at 0° C. for one hour, and was then stirred at room temperature overnight. The reaction was then stirred at 50° C. for four hours. The solution was then cooled to room temperature and added to a beaker of ice water. The ice was allowed to melt and then the solution was extracted with ethyl ether. The organic layer was washed with brine, then dried over sodium sulfate, and filtered. The solvent was removed under slightly reduced pressure to give 4-acetamido-2-fluorobenzene-1-sulfonyl chloride (1.50 g, 18% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-ebdf9e4656c14f49b9d40ee40e1da855
Source noteuspto-grants-2013_06