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HRID 572994作成日:2026年10月27日

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

https://huagongshe.com/reaction/572994

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物2-Chloro-4-nitrotolueneHCID 8491—
反応物N-bromobutanimideHCID 67184—
溶媒Carbon TetrachlorideHCID 5943—
生成物1-(Bromomethyl)-2-chloro-4-nitrobenzeneHCID 3016368—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09029533B2
出典データセットuspto-grants-2015_05
ORD IDord-a303321847cc4512bca81399b8c71c56
出典メモuspto-grants-2015_05