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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350889생성일: 2026년 10월 26일

Carbon tetrabromide → 4-bromoethyl-5-(3,5-dichloro-phenylsulfanyl)-1-ethyl-3-methyl-1 H-pyrazole

https://huagongshe.com/reaction/350889

반응식

참여 물질

역할이름HCID투입량
반응물Carbon tetrabromideHCID 11205—
반응물TriphenylphosphineHCID 11776—
반응물5-(3,5-dichloro-phenylsulphanyl)-1-ethyl-3-methyl-1H-pyrazol-4-yl-methanolHCID 22747520—
용매DichloromethaneHCID 6344—
생성물4-bromoethyl-5-(3,5-dichloro-phenylsulfanyl)-1-ethyl-3-methyl-1 H-pyrazoleHCID 6951579468.6%

반응 단계

A mixture of 460 mg of [5-(3,5-dichloro-phenylsulphanyl)-1-ethyl-3-methyl-1H-pyrazol-4-yl-]methanol, 481 mg of carbon tetrabromide and 380 mg of triphenylphosphine in 20 ml of dichloromethane was stirred at room temperature for 24 hours. The solvent was evaporated. The residue was purified by flash chromatography on silica gel using ethyl acetate/petroleum ether (bp 40–60° C.) (1:4) for the elution to give 392 mg of 4-bromoethyl-5-(3,5-dichloro-phenylsulfanyl)-1-ethyl-3-methyl-1H-pyrazole as a pale yellow oil. Mass spectrum (ES) m/z 317 [M−Br+H2O]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183296B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-ea279b84e73944f585a96bd5f54c7172
출처 메모uspto-grants-2007_02