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HRID 553922作成日:2026年10月26日

Water → ethyl (R)-2-tert-butoxycarbonylamino-5-(3,4-difluorophenyl)-5-oxovalerate

https://huagongshe.com/reaction/553922

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1-Boc-D-Pyroglutamic acid ethyl esterHCID 820885—
反応物HCID 178505835HCID 178505835—
溶媒TetrahydrofuranHCID 8028—
生成物ethyl (R)-2-tert-butoxycarbonylamino-5-(3,4-difluorophenyl)-5-oxovalerateHCID 67373437—

反応手順

To a solution of (R)-5-oxopyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (6.0 g) in tetrahydrofuran (100 mL), 3,4-difluorophenylmagnesium bromide (0.5 M solution in tetrahydrofuran; 50 mL) was added dropwise at −40° C. over 10 minutes, and the reaction solution was stirred at −40° C. to 0° C. for two hours. Water was added to the solution in small portions, followed by extraction with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to obtain 8.3 g of the title compound. The property values of the compound are as follows.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08048878B2
出典データセットuspto-grants-2011_11
ORD IDord-848be85c996c41afa02ae8fcda00e084
出典メモuspto-grants-2011_11