HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25559Generated: October 29, 2026
Ethyl Bromide → HCID 178464531, compound
https://huagongshe.com/reaction/25559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178527590 | HCID 178527590 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178464531 | HCID 178464531 | 38% |
Reaction Steps
To 4 g (12.4 mmol) trans-N-(4-Hydroxy-cyclohexyl)-4-trifluoromethyl-benzenesulfonamide in 20 ml DMF were added 5.1 g (37.1 mmol, 3.3 eq) K2CO3 and 2.04 ml (27.2 mmol, 2.2 eq) ethyl bromide. The mixture was stirred at 35° C. over night, concentrated in vacuo and dissolved in CH2Cl2 and water. The phases were separated and the inorganic one was extracted CH2Cl2, the combined organic phases were washed with brine and dried over Na2SO4. The crude product was purified by column chromatography on silica gel with CH2Cl2/MeOH 95:5 to yield 1.6 g (38%) trans-N-Ethyl-N-(4-hydroxy-cyclohexyl)-4-trifluoromethyl-benzenesulfonamide as brown oil, MS: 351(M).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858651B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-1d8749fc54a14e59a78f3c8bf8bfed5d |
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| Source note | uspto-grants-2005_02 |
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