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HRID 737075作成日:2026年10月26日

Bromoacetyl bromide → 2-Bromo-N-((S)-2-hydroxy-2-phenyl-ethyl)-acetamide

https://huagongshe.com/reaction/737075

反応式

関与物質

役割名称HCID仕込み量
反応物Bromoacetyl bromideHCID 61147—
反応物(1S)-2-amino-1-phenylethan-1-olHCID 643217—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium BicarbonateHCID 516892—
生成物2-Bromo-N-((S)-2-hydroxy-2-phenyl-ethyl)-acetamideHCID 57849523—

反応条件

温度0 °C

反応手順

To a cold (0° C.) biphasic solution of (S)-(+)-2-amino-1-phenylethanol (6.2 g, 45.2 mmol) in EtOAc (450 mL) and saturated aqueous NaHCO3 (125 mL) was added bromoacetyl bromide (4.32 mL, 49.7 mmol) via syringe. The mixture was stirred at 0° C. for 1 h then layers were separated. The aqueous layer was extracted with EtOAc (2×100 mL) then combined organics were dried with Na2SO4, filtered, and concentrated to dryness to afford the desired product as a residue (11.6 g, quant.) that was used in the next transformation: ES MS (+) m/z 258.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07595397B2
出典データセットuspto-grants-2009_09
ORD IDord-0f41999e5516492d8bc0bb872ca32808
出典メモuspto-grants-2009_09