HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484442Generated: October 31, 2026
Ammonium Hydroxide → HCID 61129737, compound
https://huagongshe.com/reaction/1484442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-Bromo-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride | HCID 58158706 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 61129737 | HCID 61129737 | 94% |
Reaction Steps
16.2 g (1 mol equiv.) 3-Bromo-4-(2,2,2-trifluoro-acetylamino)-benzenesulfonyl chloride was dissolved in 150 mL acetonitrile and cooled to 0° C. Dropwise, 20.8 mL (3 mol equiv.) ammoniumhydroxide was added and the reaction mixture was stirred at room temperature for 10 min. during which a white precipitate was formed. Volatiles were removed under reduced pressure, and the solid residue was washed with water and dried in vacuo to afford 14.3 g (94%) N-(2-bromo-4-sulfamoyl-phenyl)-2,2,2-trifluoro-acetamide. 1H NMR (400 MHz, DMSO-d6) δ 7.59 (s, 2H), 7.69 (d, J=8.2 Hz, 1H), 7.88 (dd, J=8.2, 1.8 Hz, 1H), 8.14 (d, J=1.8 Hz, 1H), 11.55 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422244B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-5c8c5523edb04d7fac5f4d69cf8d235c |
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| Source note | uspto-grants-2016_08 |
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