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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1046055생성일: 2026년 10월 25일

Acetic Acid → 4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-ol

https://huagongshe.com/reaction/1046055

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물(alphaS)-4-Bromo-alpha-methylbenzenemethanamineHCID 852999—
반응물3-Hydroxy-4-methoxy-3-phenyl-butyraldehydeHCID 59635677—
용매TetrahydrofuranHCID 8028—
생성물4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-olHCID 59635799—

반응 단계

(S)-1-(4-Bromo-phenyl)-ethylamine (0.93 g), NaB(OAc)3 (0.98 g), and acetic acid (0.27 mL) were added in the given order to a solution of 3-hydroxy-4-methoxy-3-phenyl-butyraldehyde (0.90 g) in tetrahydrofuran (20 mL) at ca. 10-15° C. The cooling bath was removed and the mixture was stirred at room temperature for 2 h. Then, water (50 mL) and 1 M aqueous NaOH solution (20 mL) were added and the resulting mixture was stirred for another 30 min. The mixture was extracted with ethyl acetate and the combined extracts were washed with water and brine. After drying (MgSO4), the solvent was removed to give the title compound which was submitted to the subsequent reaction step without further purification. Yield: 1.80 g (quantitative). Mass spectrum (ESI+): m/z=378/380 (Br) [M+H]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569292B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-1c209d81b068442eab848c615b4312c5
출처 메모uspto-grants-2013_10