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HRID 11241作成日:2026年10月23日

Benzaldehyde → (S)-2-benzylamino-3-phenyl-1-propanol

https://huagongshe.com/ja/reaction/11241

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物phenylalaninol, (S)-HCID 447213—
反応物HCID 178418361HCID 178418361—
触媒PlatinumHCID 23939—
溶媒EthanolHCID 702—
生成物(S)-2-benzylamino-3-phenyl-1-propanolHCID 1051426748.1%

反応条件

温度60 °C

反応手順

L-Phenylalaninol (5 g, 33 mmoles) and 3.59 g (33.83 mmoles) of benzaldehyde were dissolved in 55 mL of 3A ethanol under inert atmosphere in a Parr shaker and the mixture was warmed to 60° C. for 2.7 hours. The mixture was cooled to approximately 25° C. and 0.99 g of 5% platinum on carbon was added and the mixture was hydrogenated at 60 psi of hydrogen and 40° C. for 10 hours. The catalyst was filtered off, the product was concentrated under reduced pressure and the crude solid product was recrystallized from 150 mL of heptane to give 3.83 g (48% yield) of N-benzyl-L-phenylalaninol as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098202B2
出典データセットuspto-grants-2006_08
ORD IDord-44a383223fe44b849e78edd1e0e8a2be
出典メモuspto-grants-2006_08