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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1901760생성일: 2026년 10월 25일

1,3-Difluoro-5-nitrobenzene → HCID 9887211, 화합물

https://huagongshe.com/reaction/1901760

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Difluoro-5-nitrobenzeneHCID 75272—
반응물3,3-dimethyl-5-[1,2,4-triazol-1-ylmethyl]-3H-isobenzofuran-1-oneHCID 23368609—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물HCID 9887211HCID 9887211—

반응 단계

To a solution of 3,3-dimethyl-5-[1,2,4-triazol-1-ylmethyl]-3H-isobenzofuran-1-one (4.47 g Intermediate 1) in N,N-dimethylformamide (250 ml) at 0° under nitrogen was added potassium tert-butoxide (4.53 g). After one hour 3,5-difluoronitrobenzene (3.22 g) was added and stirring continued for five hours. The reaction mixture was partitioned between water and ethyl acetate and the phases separated. The aqueous phase was extracted with ethyl acetate and the combined organic extracts were washed with water and brine, dried and then evaporated to yield a brown oil. This was purified by column chromatography on Merck 9385 silica eluting initially with dichloromethane through to a 50:1 mixture of dichloromethane:methanol to yield a brown foam. The brown foam was further purified by gradient elution HPLC (water-acetonitrile-trifluoroacetic acid) to give 5-[(2,6-difluoro-4-nitrophenyl)-1,2,4-triazol-1-ylmethyl]-3,3-dimethyl-3H-isobenzofuran-1-one as a yellow foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05578630
출처 데이터셋uspto-grants-1996_11
ORD IDord-1a51447f1b804e9597a1ee27a4397a91
출처 메모uspto-grants-1996_11