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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572994생성일: 2026년 10월 26일

Azobisisobutyronitrile → 1-(Bromomethyl)-2-chloro-4-nitrobenzene

https://huagongshe.com/reaction/572994

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물2-Chloro-4-nitrotolueneHCID 8491—
반응물N-bromobutanimideHCID 67184—
용매Carbon TetrachlorideHCID 5943—
생성물1-(Bromomethyl)-2-chloro-4-nitrobenzeneHCID 3016368—

반응 단계

A suspension of 2-chloro-4-nitrotoluene (10.0 g, 58.3 mmol), N-bromosuccinimide (NBS, 10.9 g, 61.2 mmol), and 2,2′-azobis(2-methylpropionitrile) (AIBN, 0.29 g, 1.75 mmol) in 120 mL of CCl4 was heated at reflux under an atmosphere of N2 for 12 h. The reaction mixture was cooled to ambient temperature, and the solid was filtered and washed with EtOAc. The combined filtrate was washed with aq. NaHCO3, dried over Na2SO4, filtered, concentrated on rotovap, and further dried under vacuum. 1H NMR indicated the ratio of desired product to unreacted 2-chloro-4-nitrotoluene to be 50:50. This material was used directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029533B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-a303321847cc4512bca81399b8c71c56
출처 메모uspto-grants-2015_05