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HRID 267598作成日:2026年10月27日

Ethanol → Dimedone

https://huagongshe.com/reaction/267598

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物MethanolHCID 887—
反応物WaterHCID 962—
反応物5,5-Dimethyl-cyclohex-2-enone-3-olHCID 137957—
溶媒AcetoneHCID 180—
溶媒IsopropanolHCID 3776—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
溶媒Methyl Ethyl KetoneHCID 6569—
溶媒1,4-DioxaneHCID 31275—
生成物DimedoneHCID 31358—

反応条件

温度45 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03943176
出典データセットuspto-grants-1976_03
ORD IDord-daf116f38c9242cf805ee89d844d33c8
出典メモuspto-grants-1976_03