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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85211생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/85211

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물N-bromobutanimideHCID 67184—
반응물Benzene, 1-fluoro-2-methyl-4-nitro-HCID 68001—
용매Carbon TetrachlorideHCID 5943—
생성물2-(Bromomethyl)-1-fluoro-4-nitrobenzeneHCID 10353967—

반응 단계

186 g (1.20 mol) of 2-fluoro-5-nitrotoluene are dissolved in 1.2 l of carbon tetrachloride, and 214 g (1.20 mol) of N-bromosuccinimide are added. 19.7 g (120 mmol) of azodiisobutyronitrile are added, and the mixture is heated under reflux. After 16 h, the mixture is allowed to cool, filtered and evaporated to dryness under reduced pressure. The residue is dissolved in 300 ml of dichloromethane, and 300 g of sea sand are added. Once more, the mixture is then concentrated to dryness under reduced pressure, and the residue is applied to a 1 kg silica gel column. The product is chromatographed using a 20:1 mixture of cyclohexane and ethyl acetate, and the product fractions are evaporated to dryness under reduced pressure. The residue is crystallized with cyclohexane and dried under reduced pressure. This gives 92 g (32% of theory) of the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846934B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0ef82594ae314ca48f28cdfe6e947d73
출처 메모uspto-grants-2014_09