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HRID 989519作成日:2026年10月26日

Trifluoroacetic acid → (2R)-3-benzyloxy-2-aminopropanoic acid methyl ester

https://huagongshe.com/reaction/989519

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物AnisoleHCID 7519—
反応物Sodium BicarbonateHCID 516892—
反応物methyl (2R)-3-(benzyloxy)-2-{[(tert-butoxy)carbonyl]amino}propanoateHCID 54103156—
溶媒DichloromethaneHCID 6344—
生成物(2R)-3-benzyloxy-2-aminopropanoic acid methyl esterHCID 13635389—

反応手順

To a solution of tert-butyloxycarbonyl-O-benzyl-D-serine methyl ester (BF8-EZ0-275) (5.0 g, 16 mmol) stirring in dichloromethane (40 mL) and anisole (1 mL) at 0° C. was added trifluoroacetic acid (10 mL). After 4 h at room temperature, a saturated aqueous solution of sodium bicarbonate was added and the resulting mixture extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over sodium sufate, and concentrated. The crude product was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06639076B1
出典データセットuspto-grants-2003_10
ORD IDord-11cb1c7d66fa4500a13e01441aaea8c8
出典メモuspto-grants-2003_10