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HRID 85211作成日:2026年10月26日

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

https://huagongshe.com/reaction/85211

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物N-bromobutanimideHCID 67184—
反応物Benzene, 1-fluoro-2-methyl-4-nitro-HCID 68001—
溶媒Carbon TetrachlorideHCID 5943—
生成物2-(Bromomethyl)-1-fluoro-4-nitrobenzeneHCID 10353967—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846934B2
出典データセットuspto-grants-2014_09
ORD IDord-0ef82594ae314ca48f28cdfe6e947d73
出典メモuspto-grants-2014_09