Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-(2-Acetamidoethyl)benzoic acid → N-{2-[4-(Hydroxymethyl)phenyl]ethyl}acetamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-(2-Acetamidoethyl)benzoic acid | HCID 343701 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 생성물 | N-{2-[4-(Hydroxymethyl)phenyl]ethyl}acetamide | HCID 18423186 | — |
반응 단계
4-(2-Acetamidoethyl)-benzoic acid is reduced, via a mixed anhydride, with sodium borohydride to give 4-(2-acetamidoethyl)-benzyl alcohol (m.p. 72°-73° C.) and then oxidized with activated manganese dioxide to give 4-(2-acetamidoethyl)-benzaldehyde (m.p. 81°-83° C.). Subsequent reaction with malonic acid gives 4-(2-acetamidoethyl)-cinnamic acid (m.p. 206°-208° C.), which is hydrogenated to give β-[4-(2-acetamidoethyl)-phenyl]-propionic acid (m.p. 132°-133° C.). This is then subjected to acidic saponification and reacted directly with ethanol to give ethyl β-[4-(2-aminoethyl)-phenyl]-propionate hydrochloride (m.p. 165°-167° C.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04113871 |
| 출처 데이터셋 | uspto-grants-1978_09 |
| ORD ID | ord-f31cba76b74c4851be763dccff44e035 |
| 출처 메모 | uspto-grants-1978_09 |