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HRID 36504作成日:2026年10月24日

Ethyl Acetate → N-[3,3,3-Trifluoro-2-(mercaptomethyl)-1-oxopropyl]-L-leucine

https://huagongshe.com/ja/reaction/36504

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Potassium bisulfateHCID 516920—
反応物N-[2-[(Acetylthio)methyl]-3,3,3-trifluoro-1-oxopropyl]-L-leucineHCID 54059189—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
溶媒Ammonium HydroxideHCID 14923—
生成物N-[3,3,3-Trifluoro-2-(mercaptomethyl)-1-oxopropyl]-L-leucineHCID 53740741—

反応手順

A suspension of the product of Example 18 (2.3 g., 6.98 mmol.) in 4.45 mL of concentrated ammonium hydroxide and 10 mL of water was stirred at room temperature under argon for 8 minutes. The resulting clear solution was acidified with 5% potassium hydrogen sulfate solution to pH 2 and extracted with 100 mL of ethyl acetate followed by 3×75 mL of additional extractions. The combined ethyl acetate extract was washed with 100 mL of brine, dried (MgSO4) and evaporated to give 1.94 g. of an off-white solid. Flash chromatography on 200 g. of silica gel eluting with ethyl acetate: hexanes:acetic acid, 100:100:1 afforded 1.72 g. of the title isomer A product as a white crystalline solid, m.p. 143°-145° C., TLC Rf =0.38 (100:50:1 ethyl acetate:hexane:acetic acid), [α]D =-62.2° (c=1.00, methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414013
出典データセットuspto-grants-1995_05
ORD IDord-e9201d502a384a31b3a894e1357eef75
出典メモuspto-grants-1995_05