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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 918756생성일: 2026년 10월 24일

Iodine → 1-(4-chlorophenyl)-3-[(Z)-3-iodobut-2-enoxy]pyrazole

https://huagongshe.com/ko/reaction/918756

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물1-(4-Chloro-phenyl)-3-((Z)-3-tributylstannanyl-but-2-enyloxy)-1H-pyrazoleHCID 131734873—
용매DichloromethaneHCID 6344—
생성물1-(4-chlorophenyl)-3-[(Z)-3-iodobut-2-enoxy]pyrazoleHCID 89650382—

반응 단계

To 10.0 g (18.6 mmol) 1-(4-chloro-phenyl)-3-((Z)-3-tributylstannanyl-but-2-enyloxy)-1H-pyrazole in 100 ml methylene chloride have been added 4.7 g (18.6 mmol) iodine at ambient temperature with stirring which was continued for 3 h. After removal of the solvents in vacuo the crude product was dissolved in 200 ml MTBE. 100 ml 20% aqueous potassium fluoride solution have been added and the mixture was stirred for 2 h at ambient temperature. The aqueous layer was separated and extracted with 20 ml methyl-tert.-butyl ether twice. The combined organic phases have been washed twice with 20 ml of water each, dried with sodium sulfate, and the solvents were removed in vacuo. The crude product (7.2 g) has been purified by chromatography on 50 g silica with methyl-tert.-butylether/hexane (1:20). Yield 5.9 g, melting point 75-77° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09271501B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-d2ca9fdf88b74a30b3c38ffecb6e04e9
출처 메모uspto-grants-2016_03