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HRID 360030作成日:2026年10月27日

Water → tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoate

https://huagongshe.com/reaction/360030

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Diethyl EtherHCID 3283—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物Hexanoic acid, 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-oxo-, 1,1-dimethylethyl ester, (R)-(9CI)HCID 15045171—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl (R)-6-Cyano-5-hydroxy-3-oxohexanoateHCID 9794547—

反応条件

温度25 °C

反応手順

A solution of crude (R)-1,1-dimethylethyl 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3oxohexanoate, 43 g (0.126 mol) in 350 mL of tetrahydrofuran is treated with 213 mL of tetrabutylammonium fluoride solution (1.0 M in hexane). The resulting mixture is stirred for five hours, at 25° C. The mixture is treated with 500 mL of water, 300 mL of diethyl ether is added, and the layers separated. The organic layer is dried (magnesium sulfate) and then filtered through a plug of silica gel with the aid of anhydrous diethyl ether. The solvent is removed under a vacuum to obtain 21 g of crude (R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate with acceptable NMR, MS and IR spectra.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05003080
出典データセットuspto-grants-1991_03
ORD IDord-58f5e643b0c34929a98f180ed8cea65e
出典メモuspto-grants-1991_03