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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36062생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Methyl isothiocyanateHCID 11167—
반응물6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-oneHCID 14869554—
반응물Potassium tert-butoxideHCID 23665647—
용매Acetic AcidHCID 176—
생성물N-methyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamideHCID 13572009668.5%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412117
출처 데이터셋uspto-grants-1995_05
ORD IDord-de48dd21366944da9ff0804dea9a9368
출처 메모uspto-grants-1995_05