戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1418787作成日:2026年10月27日

Sodium hydride → N-benzyloxycarbonyl-3-[4-(1,4,7-trioxaoctyl)-phenyl]-alanine-methyl ester

https://huagongshe.com/reaction/1418787

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物1-Bromo-3,6-dioxaheptaneHCID 123532—
反応物Sodium BicarbonateHCID 516892—
反応物N-[(Phenylmethoxy)carbonyl]-L-tyrosine methyl esterHCID 7010613—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物N-benzyloxycarbonyl-3-[4-(1,4,7-trioxaoctyl)-phenyl]-alanine-methyl esterHCID 22940770—

反応手順

6.59 g (20 mmol) of N-benzyloxycarbonyl-tyrosine-methyl ester is dissolved in 25 ml of anhydrous N,N-dimethylformamide and mixed at 0° C. under argon with 0.81 g (20.5 mmol) of sodium hydride dispersion (60% in mineral oil). The batch is allowed to stir for 10 minutes, then 3.75 g (20.5 mmol) of 1-bromo-2-(2-methoxyethoxy)-ethane is added, the reaction temperature is allowed to increase to room temperature and stirred for another three hours. For working-up, the batch is taken up in toluene and shaken out several times against aqueous sodium bicarbonate solution. The organic phase is separated, dried on magnesium sulfate, filtered and concentrated by evaporation. The oily residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05885548
出典データセットuspto-grants-1999_03
ORD IDord-1341ac2f27f648288d7130e58f5f5e93
出典メモuspto-grants-1999_03