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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36066생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/36066

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Phenyl isocyanateHCID 7672—
반응물6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-oneHCID 14869554—
반응물Potassium tert-butoxideHCID 23665647—
용매Acetic AcidHCID 176—
생성물N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carboxamideHCID 5471968021.4%

반응 단계

To a mixture of 0.5 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-3-one, 0.39 g of potassium t-butoxide, and 5 ml of dried N,N-dimethylformamide was added dropwise a mixture of 0.42 g of phenyl isocyanate and 1.5 ml of dried N,N-dimethylformamide while stirring under cooling with ice. After stirring for 4 hours under ice-cooling, ice-water was added thereto, and the mixture was made acidic with acetic acid and extracted with diethyl ether. The ether layer was washed with water and dried over sodium sulfate. Diethyl ether was removed by distillation, and the residue was purified by silica gel column chromatography (developing solution: CH2Cl2) to obtain 0.17 g of N-phenyl-6-cyano-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carboxamide represented by formula shown below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412117
출처 데이터셋uspto-grants-1995_05
ORD IDord-66ed7a06d95b4269b26ca4cfa7ade68e
출처 메모uspto-grants-1995_05