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HRID 432205作成日:2026年10月27日

N-Methyl-N-phenylbenzylamine → N-benzyl-N-(4-bromophenyl)-N-methylamine

https://huagongshe.com/reaction/432205

反応式

関与物質

役割名称HCID仕込み量
反応物N-Methyl-N-phenylbenzylamineHCID 69191—
反応物2,4,4,6-Tetrabromocyclohexa-2,5-dienoneHCID 88433—
溶媒DichloromethaneHCID 6344—
生成物N-benzyl-N-(4-bromophenyl)-N-methylamineHCID 2234739256.7%

反応手順

N-benzyl-N-phenyl-N-methylamine (4.41 g, 0.0224 mol) was dissolved in anhydrous dichloromethane (150 mL) and 2,4,4,6-tetrabromocyclohexadiene-1-one(9.16 g, 0.0224 mol) was added in 10 equal portions over a 30 min. period. Stirring was continued at ambient temperature for 20 hours. The organic phase was successively washed with 0.5N solution of sodium hydroxide in water (100 mL), 1N solution of sodium hydroxide in water (100 mL), water (120 mL) and brine (120 mL). The organic phase was dried with magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (1:99) as mobile phase to yield N-benzyl-N-(4-bromophenyl)-N-methylamine (3.52 g, 0.0127 mol) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660744B1
出典データセットuspto-grants-2003_12
ORD IDord-b4d0e4dee0fc4432b379558712d568b2
出典メモuspto-grants-2003_12