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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1156086생성일: 2026년 10월 26일

p-Toluenesulfonic acid → 2-(2-Tetrahydrothienyl)-3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one

https://huagongshe.com/reaction/1156086

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물DimedoneHCID 31358—
반응물2,3-DihydrothiopheneHCID 136880—
용매BenzeneHCID 241—
생성물2-(2-Tetrahydrothienyl)-3-hydroxy-5,5-dimethyl-2-cyclohexen-1-oneHCID 12391648—

반응 단계

A mixture of 7 parts of dimedone, 7 parts of 2,3-dihydrothiophene, 150 parts by volume of benzene and 0.7 parts of p-toluenesulfonic acid was refluxed by heating while stirring for 1 hour and 30 minutes and then allowed to stand at room temperature for 12 hours. The reaction mixture was washed with 50 parts by volume of water and then treated three times with 50 parts by volume of a 10% aqueous solution of sodium hydroxide. The aqueous layer was collected and the pH was adjusted to 2.0 with the addition of 6 N hydrochloric acid while maintaining the temperature thereof below 10° C. The light yellow colored crystals thus deposited were collected and purified by passing through a column containing a silica gel using a solvent mixture of chloroform and benzene (1:1) as a spreading agent to obtain 2-(2-tetrahydrothienyl)-3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one in a form of colorless fine crystals. The melting point was 97° to 99° C. The yield was 8 parts.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04334010
출처 데이터셋uspto-grants-1982_06
ORD IDord-c5c81e24990d47a69c0070016df8ccff
출처 메모uspto-grants-1982_06