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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057235Generated: November 2, 2026

Ethyl Bromide → HCID 178464531, compound

https://huagongshe.com/reaction/2057235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178527590HCID 178527590—
SolventDimethylformamideHCID 6228—
ProductHCID 178464531HCID 17846453138%

Reaction Conditions

Temperature35 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335687B2
Source datasetuspto-grants-2008_02
ORD IDord-855f69f48b5f4f1f837aaaf20f0458ca
Source noteuspto-grants-2008_02