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HRID 2371作成日:2026年10月23日

Ethanol → (1S)-1-phenylethanaminium

https://huagongshe.com/ja/reaction/2371

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物2,3-Dihydroxybutanedioic AcidHCID 875—
反応物1-Phenethylamine, (-)-HCID 75818—
生成物(1S)-1-phenylethanaminiumHCID 7855572—
生成物(+)-(1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetic acidHCID 11171909—
生成物(1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetateHCID 131720568—

反応手順

This acid presented the analytical characters of the racemic acid described under b) and a [α]20D =-12° (c=1.15, ethanol) (purity: 99%; e.r. 99.2:0.8). Proceeding in a manner analogous to that described here-above, but using (-)-(S)-1-penylethylamine (Fluka purum; e.r. 98:2), there was obtained (1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetate of (S)-1-phenyl-ethylammonium (m.p. 131°-132°; [α]20D =+4°; c=1.05, ethanol) and (+)-(1R,2S,3R)-3-hydroxy-2-pentyl-1-cyclopentaneacetic acid having [α]20D =+11° (c=1.10, ethanol) (purity: 99%; e.r. 96.5:3.5).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728866
出典データセットuspto-grants-1998_03
ORD IDord-9351ff791ece43d89068d7c5e43ad1d4
出典メモuspto-grants-1998_03