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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1085603생성일: 2026년 10월 27일

Pyrrole → 4,5-Dichloro-2-(3,4-dichlorophenyl)-1-(2-hydroxyethyl)-pyrrole-2-carbonitrile

https://huagongshe.com/reaction/1085603

반응식

참여 물질

역할이름HCID투입량
반응물PyrroleHCID 8027—
반응물4,5-dichloro-2-(3,4-dichlorophenyl)-1H-pyrrole-3-carbonitrileHCID 183555—
반응물Ethanol, 1-bromo-HCID 14202443—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물4,5-Dichloro-2-(3,4-dichlorophenyl)-1-(2-hydroxyethyl)-pyrrole-2-carbonitrileHCID 19026377—

반응 단계

To a stirred mixture of 2.0 g (6.5 mmol) of 4,5-dichloro-2-(3,4-dichlorophenyl)-pyrrole-3-carbonitrile and 0.88 g (7.8 mmol) of potassium tert-butoxide heated at reflux in 50 mL of dioxane is added 0.98 g (7.8 mmol) of bromoethanol. The mixture is stirred at reflux for 12 hours, cooled, diluted with 50 mL of water, and extracted several times with chloroform. The combined chloroform extracts are dried over magnesium sulfate and concentrated in vacuo to leave a solid which, on warming and dissolving in ethyl acetate, deposits on cooling mostly starting pyrrole. Concentration of the mother liquor and recrystallization of the residual solid from 20% ethyl acetate in hexane gives 0.31 g of a white solid, mp 143°-145° C.; IR 5077A.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05010098
출처 데이터셋uspto-grants-1991_04
ORD IDord-7c6a8238d4b340fea450e95059ce81ba
출처 메모uspto-grants-1991_04