Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927985Generated: October 30, 2026

Chlorosulfonic acid → 4-Fluoro-2-(trifluoroacetylaminomethyl)benzenesulfonyl chloride

https://huagongshe.com/reaction/927985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant3-Fluoro-N-trifluoroacetylbenzylamineHCID 62492148—
Product4-Fluoro-2-(trifluoroacetylaminomethyl)benzenesulfonyl chlorideHCID 86713320—

Reaction Conditions

Temperature70 °C

Reaction Steps

3-Fluoro-N-trifluoroacetylbenzylamine (Intermediate 105, 1.11 g) was added portionwise to chlorosulfonic acid (5 mL), while stirring and cooling in an ice bath. On completion of the addition, the ice bath was removed and the mixture was allowed to come to room temperature then heated to 70° C. for 3 hours. After cooling, the mixture was slowly added to ice and the resultant suspension was extracted with ethyl acetate, washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give 4-fluoro-2-(trifluoroacetylaminomethyl)benzenesulfonyl chloride (1.53 g) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-a5b1c0dd3dab46a2bff280948a2c43a7
Source noteuspto-grants-2016_03