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HRID 36062作成日:2026年10月24日

Dimethylformamide → N-methyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide

https://huagongshe.com/ja/reaction/36062

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Methyl isothiocyanateHCID 11167—
反応物6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-oneHCID 14869554—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Acetic AcidHCID 176—
生成物N-methyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamideHCID 13572009668.5%

反応手順

To a mixture of 1.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-one, 0.6 g of methyl isothio-cyanate, and 15 ml of dried N,N-dimethylformamide was added 0.93 g of potassium t-butoxide with stirring under ice-cooling, followed by stirring for 4 hours under ice-cooling. Ice-water was added to the reaction mixture, and the mixture was made acidic with acetic acid and then extracted with diethyl ether. The ether layer was washed with water and dried over sodium sulfate. The ether layer was removed by distillation, and the residue was recrystallized from ethanol to yield 1.4 g of N-methyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide represented by formula shown below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05412117
出典データセットuspto-grants-1995_05
ORD IDord-de48dd21366944da9ff0804dea9a9368
出典メモuspto-grants-1995_05