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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1984473생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1984473

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 번호US07544697B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-8d224dfa6603409f8a57f8d832e80a00
출처 메모uspto-grants-2009_06