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HRID 889682作成日:2026年10月25日

Tetrahydrothiophene → 2-Phenyl-1-oxaspiro[2.5]octane

https://huagongshe.com/reaction/889682

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrothiopheneHCID 1127—
反応物Benzyl ChlorideHCID 7503—
反応物CyclohexanoneHCID 7967—
反応物Potassium HydroxideHCID 14797—
反応物S-benzyltetrahydrothiophenium chlorideHCID 86626231—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物2-Phenyl-1-oxaspiro[2.5]octaneHCID 25481481.5%

反応条件

温度20 °C

反応手順

A mixture of 152 g (1.18 mol) of benzyl chloride, 108 g (1.18 mol) of tetrahydrothiophene and 0.225 L of water is stirred well at 85° C. until a homogeneous clear or slightly turbid single-phase solution of S-benzyltetrahydrothiophenium chloride has been obtained. The solution is cooled to 20° C. and is slowly added dropwise to a reaction mixture consisting of potassium hydroxide solution (prepared from 267 g (4.75 mol) of potassium hydroxide in 0.53 L of ice-water) and 467 g of cyclohexanone (4.75 mol) in 225 g of methanol. After the addition is complete, the reaction mixture is allowed to stand for 10 minutes until the phases have separated; the organic phase is separated off and subjected to fractional distillation. 181 g (80%) of 2-phenyl-1-oxa-spiro[2.5]octane are obtained in the form of a clear colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08252959B2
出典データセットuspto-grants-2012_08
ORD IDord-a08d88969042452693127dbad0239381
出典メモuspto-grants-2012_08