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HRID 11605作成日:2026年10月26日

Triethylamine → (S)-2-(4-fluoro-benzylamino)-propionic acid methyl ester

https://huagongshe.com/reaction/11605

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物4-FluorobenzaldehydeHCID 68023—
反応物Alanine methyl ester hydrochlorideHCID 2733257—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
生成物(S)-2-(4-fluoro-benzylamino)-propionic acid methyl esterHCID 4323025091%

反応手順

To a solution of (S)-2-amino-propionic acid methyl ester hydrochloride (25 g, 179 mmol) and 4-fluorobenzaldehyde (23 mL, 215 mmol) in 1,2-dichloroethane (200 mL) was added triethylamine (25 mL, 179 mmol). The resulting mixture was stirred for two hours at ambient temperature followed by addition of sodium triacetoxyborohydride (57 g, 268 mmol) in four portions. The resulting mixture was stirred overnight at ambient temperature. The reaction was neutralized with dilute aqueous sodium hydroxide solution and extracted with dichloromethane. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. Chromatography on silica gel gave the title compound (34.4 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098212B2
出典データセットuspto-grants-2006_08
ORD IDord-06705e7a1e0948f294c7e03ad98290a8
出典メモuspto-grants-2006_08