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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 3-Fluoro-N-trifluoroacetylbenzylamine | HCID 62492148 | — |
| Product | 4-Fluoro-2-(trifluoroacetylaminomethyl)benzenesulfonyl chloride | HCID 86713320 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290472B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-a5b1c0dd3dab46a2bff280948a2c43a7 |
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| Source note | uspto-grants-2016_03 |
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