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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 553297생성일: 2026년 10월 25일

2-(2-Fluorophenyl)ethylamine → (3-{[2-(2-Fluoro-phenyl)-ethylamino]-methyl}-4-methoxy-phenyl)-acetic acid methyl ester

https://huagongshe.com/reaction/553297

반응식

참여 물질

역할이름HCID투입량
반응물2-(2-Fluorophenyl)ethylamineHCID 643357—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(3-Formyl-4-methoxy-phenyl)-acetic acidHCID 23025459—
용매DichloromethaneHCID 6344—
생성물(3-{[2-(2-Fluoro-phenyl)-ethylamino]-methyl}-4-methoxy-phenyl)-acetic acid methyl esterHCID 6716593170%

반응 단계

2-(2-Fluorophenyl)ethylamine (180 mg) in dichloromethane (5 mL) was added to (3-formyl-4-methoxy-phenyl)-acetic acid (260 mg). After 30 minutes, sodium triacetoxyborohydride (0.5 g) was added. After a further 2.5 hours, the reaction mixture was evaporated and the residue loaded onto a conditioned SCX cartridge (10 g Varian). The cartridge was washed with methanol (50 mL) and then eluted with a mixture of methanol/0.880 ammonia solution [4:1] (50 mL). The elution fraction was concentrated, the residue was dissolved in methanol (100 mL) and tri-methylchlorosilane (2 mL) added. After 18 hours, the reaction mixture was evaporated and the residue purified on silica, eluting iso-hexane/ethyl acetate [4:1 to 1:1 to 0:1]+1% triethylamine, to give the subtitle compound as an oil (0.30 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951954B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-c22fde2850814a238098d9997ddc0a12
출처 메모uspto-grants-2011_05