돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345560생성일: 2026년 10월 24일

1,4-Cyclohexanediol → HCID 15096979, 화합물

https://huagongshe.com/ko/reaction/345560

반응식

참여 물질

역할이름HCID투입량
반응물1,4-CyclohexanediolHCID 11162—
반응물Sodium hydrideHCID 24758—
반응물2,5-DifluoronitrobenzeneHCID 67767—
용매DimethylformamideHCID 6228—
생성물HCID 15096979HCID 15096979—

반응 단계

To a stirred mixture of 46.46 parts of 1,4-cyclohexanediol and 135 parts of N,N-dimethylformamide were added 5.28 parts of sodium hydride dispersion 50% at a temperature below 20° C. Stirring was continued for 2 hours at room temperature under nitrogen atmosphere. Then there were added dropwise 15.9 parts of 1,4-difluoro-2-nitrobenzene at about 20° C. Upon completion, stirring was continued overnight at room temperature. The reaction mixture was poured onto water. The precipitated product was filtered off and taken up in trichloromethane. The solution was washed with water, dried, filtered and evaporated. The residue was boiled in 2-propanol. Upon cooling, the precipitate was filtered off and the filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was stirred in petroleumether. The product was filtered off and dried, yielding 17.1 parts of 4-(4-fluoro-2-nitrophenoxy)cyclohexanol; mp. 150.8° C. (intermediate 85).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05057525
출처 데이터셋uspto-grants-1991_10
ORD IDord-cda535e558c14d91881ce6da9ba147d0
출처 메모uspto-grants-1991_10