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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30232생성일: 2026년 10월 23일

Ammonium Acetate → 1-[4-(4-Trifluoromethoxy-benzyloxy)-phenyl]-ethylamine

https://huagongshe.com/ko/reaction/30232

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1-[4-(4-Trifluoromethoxybenzyloxy)phenyl]ethanoneHCID 52561273—
용매MethanolHCID 887—
생성물1-[4-(4-Trifluoromethoxy-benzyloxy)-phenyl]-ethylamineHCID 5862902869.4%

반응 조건

온도50 °C

반응 단계

To a mixture of 552.0 mg (1.779 mmol) 1-[4-(4-trifluoromethoxy-benzyloxy)-phenyl]-ethanone and molecular sieves in 10 ml methanol were added 1679.0 mg (21.35 mmol) ammonium acetate and 78.0 mg (1.241 mmol) sodium cyanoborohydride and the reaction mixture was stirred 26 h (HPLC control) at 50° C. After cooling to room temperature, the molecular sieves were filtered off and washed with methanol. The solvent of the combined filtrates was evaporated and diethyl ether and water were added to the residue. While stirring the mixture was acidified with 6N aqueous HCl solution to pH2. The aqueous phase was separated and the organic phase was extracted two times with 1N aqueous HCl solution. Ethyl acetate was added to the combined aqueous phases and the mixture was basified with 6N NaOH to pH 10. The organic phase was separated and the aqueous phase was extracted two more times with ethyl acetate. The combined organic phases were dried over MgSO4 and the solvent evaporated at reduced pressure to afford 268.0 mg (0.861 mmol) 1-[4-(4-trifluoromethoxy-benzyloxy)-phenyl]-ethylamine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423060B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-55298638a57f4a4094f88fe78e947bd1
출처 메모uspto-grants-2008_09