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HRID 1359151作成日:2026年10月26日

N-bromobutanimide → 6'-Methyl-2'-bromomethyl-2-(4-methoxybenzoyl)-biphenyl-4-carbonitrile

https://huagongshe.com/reaction/1359151

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物4'-Methoxy-2',6'-dimethyl-2-(4-methoxybenzoyl)-biphenyl-4-carbonitrileHCID 10894011—
反応物Nbs aibnHCID 86630000—
触媒AzobisisobutyronitrileHCID 6547—
溶媒Carbon TetrachlorideHCID 5943—
生成物6'-Methyl-2'-bromomethyl-2-(4-methoxybenzoyl)-biphenyl-4-carbonitrileHCID 1818274893.6%

反応手順

To a refluxing solution of the compound from Step D (45.5 g, 122 mmol) and AIBN (1.0 g) in CCl4 (2.5 L) was added a mixture of NBS (23.0 g, 129 mmol) and AIBN (1.0 g) in ten equal portions. The reaction mixture was refluxed for 2 h after the addition of the last portion of NBS/AIBN. The reaction mixture was concentrated to approximately 1 L and washed 3 times with water (1 L). The organic layer was dried with anhydrous Na2SO4, filtered and the solvent removed. Toluene (200 ml) was added to the residue and then evaporated. Repeating this procedure gave 48 g of the title compound that was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06599921B2
出典データセットuspto-grants-2003_07
ORD IDord-3ec49c2663994f3995567c06e06a9d32
出典メモuspto-grants-2003_07