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HRID 889682생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/889682

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrothiopheneHCID 1127—
반응물Benzyl ChlorideHCID 7503—
반응물CyclohexanoneHCID 7967—
반응물Potassium HydroxideHCID 14797—
반응물S-benzyltetrahydrothiophenium chlorideHCID 86626231—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물2-Phenyl-1-oxaspiro[2.5]octaneHCID 25481481.5%

반응 조건

온도20 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08252959B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-a08d88969042452693127dbad0239381
출처 메모uspto-grants-2012_08