HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842986Generated: October 31, 2026
Ethanesulfonyl chloride → N-(4-bromo-2-fluorobenzyl)ethanesulfonamide
https://huagongshe.com/reaction/1842986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | (4-Bromo-2-fluorophenyl)methanamine | HCID 3770848 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(4-bromo-2-fluorobenzyl)ethanesulfonamide | HCID 70816043 | — |
Reaction Steps
4-Bromo-2-fluorobenzylamine (924 mg, 4.53 mmol) was dissolved in pyridine and ethane sulfonyl chloride (0.82 mL, 8.60 mmol) was added to the solution at 0° C. The mixture was stirred for 1 h at 0° C. Then, the mixture was quenched with 1N HCl and extracted with ethyl acetate (EtOAc). Drying (MgSO4) and evaporation of the ethyl acetate followed and the residue was purified by CC (eluent EtOAc/n-hexane) to yield N-(4-bromo-2-fluorobenzyl)ethanesulfonamide in pure form (1.06 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946204B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-ca39859f1b1f47f09ed664ed68c9e331 |
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| Source note | uspto-grants-2015_02 |
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