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HRID 36522作成日:2026年10月26日

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

https://huagongshe.com/reaction/36522

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US05414017
出典データセットuspto-grants-1995_05
ORD IDord-8c00c1c5406948469c800a9fa1906d65
出典メモuspto-grants-1995_05