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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72369생성일: 2026년 10월 24일

Ammonium Acetate → N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide

https://huagongshe.com/ko/reaction/72369

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물N-(tert-Butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamideHCID 68288463—
용매MethanolHCID 887—
생성물N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamideHCID 68287917—

반응 단계

A solution of 0.66 g of N-(tert-butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide, 1.85 g of ammonium acetate and 0.17 g of sodium cyanoborohydride in 12 ml of methanol was stirred at 60° C. for 17 hours. After the removal of the solvent under reduced pressure, the residue was taken up in 50 ml of ethyl acetate and washed twice with 30 ml of 0.5 N aqueous sodium hydroxide solution and 30 ml of saturated aqueous sodium chloride solution. The organic phase was dried over MgSO4 and concentrated by rotary evaporation. The crude product was subjected to a chiral separation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828994B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-862b77b448334435a0c2e674fe13fedc
출처 메모uspto-grants-2014_09