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HRID 1732652作成日:2026年10月27日

4-(2-Acetamidoethyl)benzoic acid → N-{2-[4-(Hydroxymethyl)phenyl]ethyl}acetamide

https://huagongshe.com/reaction/1732652

反応式

関与物質

役割名称HCID仕込み量
反応物4-(2-Acetamidoethyl)benzoic acidHCID 343701—
反応物Sodium borohydrideHCID 4311764—
生成物N-{2-[4-(Hydroxymethyl)phenyl]ethyl}acetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04238506
出典データセットuspto-grants-1980_12
ORD IDord-30f9ba0e2e5240c8bb89b8d779faa7f5
出典メモuspto-grants-1980_12