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HRID 36065作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/36065

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Phenyl IsothiocyanateHCID 7673—
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-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamideHCID 13572009947.9%

反応手順

To a mixture of 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-one, 0.37 g of phenyl isothio-cyanate, and 5 ml of dried N,N-dimethylformamide was added 0.31 g of potassium t-butoxide with under ice-cooling, followed by stirring for 5 hours under ice-cooling. Ice-water was added thereto, and the mixture was made acidic with acetic acid and extracted with diethyl ether. The extract was washed with water and dried over sodium sulfate, and the ether layer was removed by distillation. The residue was purified by silica gel column chromatography (developing solution: CH2Cl2) to obtain 0.4 g of N-phenyl-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-5b12e05a7622475082ec0de4fcdad81a
出典メモuspto-grants-1995_05