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4-(2-Acetamidoethyl)benzoic acid → N-{2-[4-(Hydroxymethyl)phenyl]ethyl}acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-(2-Acetamidoethyl)benzoic acid | HCID 343701 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 生成物 | N-{2-[4-(Hydroxymethyl)phenyl]ethyl}acetamide | HCID 18423186 | — |
反応手順
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.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04238506 |
| 出典データセット | uspto-grants-1980_12 |
| ORD ID | ord-30f9ba0e2e5240c8bb89b8d779faa7f5 |
| 出典メモ | uspto-grants-1980_12 |