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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 857474생성일: 2026년 10월 26일

Azobisisobutyronitrile → 4-Bromomethyl-1-(2-chloro-phenyl)-5-(4-chloro-phenyl)-1H-pyrazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/857474

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물Ethyl 1-(2-chlorophenyl)-5-(4-chlorophenyl)-4-methyl-1h-pyrazole-3-carboxylateHCID 58760952—
용매Carbon TetrachlorideHCID 5943—
생성물4-Bromomethyl-1-(2-chloro-phenyl)-5-(4-chloro-phenyl)-1H-pyrazole-3-carboxylic acid ethyl esterHCID 5876094664%

반응 단계

A mixture of 1-(2-chloro-phenyl)-5-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-carboxylic acid ethyl ester I-4a (2.8 g, 7.46 mmol), N-bromosuccinimide (1.6 g, 8.95 mmol), AIBN (245 mg, 1.49 mmol) in CCl4 (60 ml) was heated under reflux for 17 hours. The reaction was cooled to room temperature, filtered to remove any solids, and concentrated under vacuum. The crude residue was purified via silica gel chromatography (Flash 40) using a solvent gradient of 10% EtOAc/hexanes to 20% EtOAc/hexanes to give the desired product (I-4b) as an amorphous solid (2.2 g, 64%): +APCI MS (M+1) 455.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07145012B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-b34d8f3bfdd646a2959e9946e220144c
출처 메모uspto-grants-2006_12