돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 901607생성일: 2026년 10월 23일

Hydrochloric Acid → N-Cyclohexyl-3-(hydroxymethyl)benzenesulfonamide

https://huagongshe.com/ko/reaction/901607

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물MethanolHCID 887—
반응물3-(Cyclohexylsulfamoyl)benzoic acidHCID 779108—
반응물Borane;tetrahydrofuranHCID 2723981—
용매TetrahydrofuranHCID 8028—
생성물N-Cyclohexyl-3-(hydroxymethyl)benzenesulfonamideHCID 6575161990.9%

반응 단계

A solution of 3-[(cyclohexylamino)sulfonyl]benzoic acid (2.25 g) in THF (100 ml) under nitrogen at 0° was treated dropwise with 1M borane-THF solution (23.82 ml). The mixture was stirred at 0° for 0.5 h and then at 20° for 72 h. The mixture was cooled to 0° and MeOH (20 ml) was added dropwise. The mixture was stirred for 15 min and then 2N hydrochloric acid (50 ml) was added and the mixture was allowed to warm to 20°. The bulk of the organic solvents were removed by evaporation in vacuo and the residual aqueous phase was extracted with EtOAc (2×40 ml). The combined extracts were dried (Na2SO4) and the solvent evaporated in vacuo. The residue was purified by SPE on alumina (10 g, activated, neutral, Brockmann 1). Elution with MeOH-dichloromethane (1:20) gave the title compound (1.944 g). LCMS RT=2.95 min, ES+ve 270 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07361787B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-4abfbf4a22124134aa698c3505cef319
출처 메모uspto-grants-2008_04