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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57466생성일: 2026년 10월 24일

Phenol → (1S)-1-(3-phenoxyphenyl)ethan-1-amine

https://huagongshe.com/ko/reaction/57466

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참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Cesium carbonateHCID 10796—
반응물1-(Pyridin-2-yl)propan-2-oneHCID 95910—
반응물(S)-1-(3-bromophenyl)ethanamineHCID 9952938—
용매Dimethyl SulfoxideHCID 679—
생성물(1S)-1-(3-phenoxyphenyl)ethan-1-amineHCID 8673019550.5%

반응 조건

온도90 °C

반응 단계

Into a 20 ml microwave vial was weighted 1-(pyridin-2-yl)propan-2-one ligand (90 mg, 0.665 mmol), phenol (407 mg, 4.32 mmol), CuBr (47.7 mg, 0.332 mmol) and Cs2CO3 (2166 mg, 6.65 mmol). To the mixture was added DMSO (5 ml) and (S)-1-(3-bromophenyl)ethanamine (0.5 ml, 3.32 mmol). The tube was flushed with N2, capped, and the black mixture heated in the oil bath at 90° C. for 18 hours. The heterogenous mixture was diluted with EtOAc and filtered through a glass-fritted funnel, eluting with EtOAc and another 5 mls of DMSO. The volatiles were then removed in vacuo and the crude brown liquid was filtered through 1 um PTFE filter and purified by reverse phase HPLC. The combined product fractions were desalted by addition of equal amount of EtOAc and about 250 mg Na2CO3 in a separatory funnel. The phases were separated and the organic washed with brine, dried over MgSO4, filtered and concentrated in vacuo to yield (S)-1-(3-phenoxyphenyl)ethanamine (361.5 mg, 1.678 mmol, 50.5% yield) as an amber oil. LCMS m/z 214.1 (M+H)+, Rt 0.61 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-327ccacb149a47d1b5aaa45de1a3b243
출처 메모uspto-grants-2016_09