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HRID 328073作成日:2026年10月24日

Water → Tert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoate

https://huagongshe.com/ja/reaction/328073

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物HexaneHCID 8058—
反応物Cyclopentyl methyl ketoneHCID 22326—
反応物1,1-Dimethylethyl dichloroacetateHCID 3016483—
溶媒TetrahydrofuranHCID 8028—
生成物Tert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoateHCID 21443888—

反応条件

温度-30 °C

反応手順

A mixture of 12.3 g of cyclopentylmethyl ketone and 18.5 g of tert.-butyl dichloroacetate was cooled to -30° C with stirring under an inert atmosphere and a solution of 12.2 g of potassium tert.-butylate in 60 ml of tetrahydrofuran was added thereto at the said temperature. After returning to room temperature, hexane and water were added and the organic phase was separated, washed with water and dried over magnesium sulfate. The solvents were evaporated off to leave an oily residue of tert.-butyl 2-chloro-3-cyclopentyl-2,3-epoxy-butanoate. 26.5 g of the latter product was added to a solution of 3 g of lithium carbonate and 20 g of lithium bromide in 100 ml of hexamethylphosphorotriamide and after stirring for 1 hour at room temperature, petroleum ether and water were added thereto. The organic phase was washed with water, dried over magnesium sulfate and filtered. The solvent was evaporated to obtain an oily residue which was tert.-butyl 3-cyclopentyl-2-oxo-3-butenoate which was used as is for the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04016158
出典データセットuspto-grants-1977_04
ORD IDord-5efebaedd46c470e8f15e08ae676c09b
出典メモuspto-grants-1977_04