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HRID 275878作成日:2026年10月27日

Acetic Acid → 2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol

https://huagongshe.com/reaction/275878

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物3,4-Bis(benzyloxy)benzaldehydeHCID 79526—
反応物2-Amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 54358865—
反応物HCID 178511851HCID 178511851—
溶媒MethanolHCID 887—
生成物2-(3,4-Dibenzyloxybenzyl)amino-5-chloro-alpha-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcoholHCID 5442387875.5%

反応条件

温度60 °C

反応手順

In methanol (20 ml) were dissolved 2-amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.6 g) and 3,4-dibenzyloxybenzaldehyde (0.55 g). To the solution were added acetic acid (0.12 g) and cyano sodium borohydride (0.13 g). The mixture was stirred for 1.5 hour at 60° C. The reaction mixture was concentrated, to which were added water (50 ml) and ethyl acetate (80 ml), followed by extraction. The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 2-(3,4-dibenzyloxybenzyl)amino-5-chloro-α-(3-tert-butoxycarbonylaminomethylphenyl)benzyl alcohol (0.83 g) as colorless crystals, m.p.: 118-120° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352982B1
出典データセットuspto-grants-2002_03
ORD IDord-f1156755ca1643af932a9577860a226c
出典メモuspto-grants-2002_03