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HRID 2266598作成日:2026年10月25日

tert-Butanol → 2-[4-(morpholine-4-sulfonyl)benzyl]-3-oxopentanoic Acid Methyl Ester

https://huagongshe.com/reaction/2266598

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物Methyl 3-oxovalerateHCID 121699—
反応物4-((4-(Bromomethyl)phenyl)sulfonyl)morpholineHCID 2779680—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物2-[4-(morpholine-4-sulfonyl)benzyl]-3-oxopentanoic Acid Methyl EsterHCID 68784251—

反応条件

温度0 °C

反応手順

A suspension of potassium tert-butoxide (0.26 g) in anhydrous tetrahydrofuran (40 mL) at 0° C. was treated with a mixture of tert-butanol (1.0 mL) and 3-oxopentanoic acid methyl ester (0.25 mL). The mixture was stirred at 0° C. for 45 minutes and then a solution of 4-(4-bromomethylbenzenesulfonyl)morpholine (0.53 g) in tetrahydrofuran (10 mL) was added and the resulting mixture warmed to room temperature over 1 hour and then stirred at this temperature for 17 hours. The mixture was concentrated under reduced pressure and the residue diluted with water and extracted with ethyl acetate. The combined extracts were washed with saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography on silica gel, eluting with a mixture of ethyl acetate and cyclohexane (1:1 by volume) to afford title compound, 0.41 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07858640B2
出典データセットuspto-grants-2010_12
ORD IDord-3eae3e8443ad4797b7246d6098f91502
出典メモuspto-grants-2010_12