돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36065생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Phenyl IsothiocyanateHCID 7673—
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-carbothioamideHCID 13572009947.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05412117
출처 데이터셋uspto-grants-1995_05
ORD IDord-5b12e05a7622475082ec0de4fcdad81a
출처 메모uspto-grants-1995_05