돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 267598생성일: 2026년 10월 27일

Ethanol → Dimedone

https://huagongshe.com/reaction/267598

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물MethanolHCID 887—
반응물WaterHCID 962—
반응물5,5-Dimethyl-cyclohex-2-enone-3-olHCID 137957—
용매AcetoneHCID 180—
용매IsopropanolHCID 3776—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
용매Methyl Ethyl KetoneHCID 6569—
용매1,4-DioxaneHCID 31275—
생성물DimedoneHCID 31358—

반응 조건

온도45 °C

반응 단계

A mixture of 3-hydroxy-5,5-dimethyl-2-cyclohexen-1-one (dimedone), and R1 -thiolsulfonate, an alkali metal hydroxide, water and a water-miscible solvent, i.e., methanol, ethanol, 2-propanol, acetone, methyl ethyl ketone, dimethylformamide, dioxane or acetonitrile, is heated with stirring at any temperature between about 45°C. and the boiling temperature of the aqueous solvent (preferably at the boiling temperature) for a period of time of about one hour to about 48 hours (preferably three to 24 hours). After the reaction, the solvent mixture is removed by evaporation or by distillation. The residue is washed with water to remove the sulfinate salt by-product, and the crude product is collected on a filter and dried. Purification is accomplished by recrystallizing the crude product from an organic solvent, i.e., a hydrocarbon or lower alkanol such as benzene, cyclohexane, n-hexane, methylcyclohexane, n-pentane, ethanol, aqueous ethanol, methanol, aqueous methanol or toluene or a combination thereof.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03943176
출처 데이터셋uspto-grants-1976_03
ORD IDord-daf116f38c9242cf805ee89d844d33c8
출처 메모uspto-grants-1976_03