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HRID 25681作成日:2026年10月26日

Triethylamine → tert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetate

https://huagongshe.com/reaction/25681

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物tert-Butyl bromoacetateHCID 79177—
反応物2-Amino-2-phenylethan-1-olHCID 134797—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetateHCID 5906586933%

反応手順

Following the literature procedure (Panek, J., J. Org. Chem., 1998, 63, 2382), triethylamine (6.2 ml, 44.5 mmole) was added to a solution of (S)-phenylglycinol (5 g, 36.45 mmole) in anhydrous tetrahydrofuran (150 ml) under argon at 0° C. After stirring for 15 min, tert-butyl bromoacetate (5.9 ml, 39.96 mmole) was added slowly to this cooled solution. The resulting mixture was warmed to room temperature, and stirred for 15 h. Saturated ammonium chloride aqueous solution was added, and the aqueous layer was extracted with diethyl ether (3 times). The combined extracts were washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to dryness in vacuo. The resulting solid was recrystallized from a diethyl ether/n-hexane mixture to give tert-butyl (S)-(2-Hydroxy-1-phenyl-ethylamino)-acetate as a white solid (3 g, 33%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858591B2
出典データセットuspto-grants-2005_02
ORD IDord-4155ccae976a4f078fbd239bf2b9a877
出典メモuspto-grants-2005_02