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HRID 242772作成日:2026年10月25日

Aniline → (3-Methyl-2-nitrophenyl)phenylamine

https://huagongshe.com/reaction/242772

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物Cesium carbonateHCID 10796—
反応物Benzene, 1-bromo-3-methyl-2-nitro-HCID 142929—
触媒palladium(II) acetateHCID 167845—
触媒Binap, (A+-)-HCID 634876—
溶媒TolueneHCID 1140—
生成物(3-Methyl-2-nitrophenyl)phenylamineHCID 1070453488.1%

反応条件

温度110 °C

反応手順

A mixture of 1-bromo-3-methyl-2-nitrobenzene (1 g, 4.63 mmol), phenylamine (422 μL, 4.63 mmol), Cs2CO3 (2.11 g, 6.48 mmol) and (R)-BINAP (5 mol %, 143 mg, 0.23 mmol) in toluene (20 mL) was degassed with a stream of nitrogen prior to addition of Pd(OAc)2 (25 mg, 0.11 mmol) and was stirred at 110° C. under a nitrogen atmosphere for 18 h. After cooling to RT, the mixture was partitioned between EtOAc and water. The organic layer was washed with brine, then dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-35% DCM in cyclohexane) affording (3-Methyl-2-nitrophenyl)phenylamine as a red oil (931 mg, 88%). LCMS: RT 3.97 min [M+H]+ 229.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653089B2
出典データセットuspto-grants-2014_02
ORD IDord-6970c8b8c212497992ab4d54a1cb1d73
出典メモuspto-grants-2014_02