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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-(2-Fluorophenyl)ethylamine | HCID 643357 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 반응물 | (3-Formyl-4-methoxy-phenyl)-acetic acid | HCID 23025459 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (3-{[2-(2-Fluoro-phenyl)-ethylamino]-methyl}-4-methoxy-phenyl)-acetic acid methyl ester | HCID 67165931 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07951954B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-c22fde2850814a238098d9997ddc0a12 |
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| 출처 메모 | uspto-grants-2011_05 |
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