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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2283873생성일: 2026년 10월 27일

Bromine → 5-(3-benzenesulfonylpropyl)4-bromo-1-butyl-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/2283873

반응식

참여 물질

역할이름HCID투입량
반응물BromineHCID 24408—
반응물Sodium ThiosulfateHCID 24477—
반응물Potassium AcetateHCID 517044—
반응물5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carbonitrileHCID 66958321—
용매Acetic AcidHCID 176—
생성물5-(3-benzenesulfonylpropyl)4-bromo-1-butyl-1H-pyrazole-3-carbonitrileHCID 6695859945.2%

반응 단계

Potassium acetate (3.82 g, 38.9 mmol) was added to a solution of 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carbonitrile (8.60 g, 25.9 mmol) in 50 mL of acetic acid. The reaction mixture was stirred until all solids had dissolved, followed by dropwise addition of bromine (1.33 mL, 25.9 mmol) over 5 minutes. The resultant red solution was stirred for 5 hours and aqueous sodium thiosulfate was added to quench excess bromine. The reaction mixture was concentrated under reduced pressure and the residue was diluted with 200 mL of water. The pH of the mixture was adjusted to 8-9 by slow addition of solid sodium carbonate followed by extraction with several portions of ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to afford an orange oil. Purification via flash column chromatography on silica gel (eluting with hexane:ethyl acetate in a gradient from 3:1 to 1:1) afforded 4.80 g of 5-(3-benzenesulfonylpropyl)-4-bromo-1-butyl-1H-pyrazole-3-carbonitrile as a colorless oil that crystallized upon standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09145410B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-f2b49ef22c9e45939b0abd80f9100798
출처 메모uspto-grants-2015_09