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HRID 1387704作成日:2026年10月27日

Toluene → 2,2'-Dimethylbiphenyl

https://huagongshe.com/reaction/1387704

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物3,5-DimethylchlorobenzeneHCID 32887—
反応物N-MethylheptylamineHCID 93190—
反応物Sodium t-butoxideHCID 23676156—
触媒PalladiumHCID 23938—
触媒(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
溶媒Diethyl EtherHCID 3283—
生成物2,2'-DimethylbiphenylHCID 11797126.1%

反応条件

温度105 °C

反応手順

This is an example of Pd/ligand 4-catalyzed aryl amination reaction for aryl amine synthesis. A reaction tube containing NaOtBu (120 mg, 1.25 mmol) was thoroughly evacuated and purged with argon. 5-Chloro-m-xylene (0.14 mL, 1.04 mmol), heptylmethylamine (0.21 mL, 1.25 mmol), a toluene solution of Pd(dba)2 (1.2 mL, 1.0 mg/mL, 2.1 μmol) and a toluene solution of ligand 4 (2.5 mL, 1.0 mg/mL, 6.2 ,μmol) and toluene (0.3 mL) were added to the reaction tube and the reaction was heated at 105° C. for 21.5 h. The reaction was taken up in ether (100 mL) and washed with H2O (30 mL) and brine (30 mL). The organic phase was dried over MgSO4, filtered and concentrated under vacuum. The crude product was purified by column chromatography on silica gel using hexanes/ethyl acetate as eluant to afford compound 2 (shown below in Table 1) as a yellowish oil (239 mg, 98%) after drying under vacuum. 1 H NMR (CDCl3): δ6.33 (br, 3H, ArH), 3.25 (t, J=7.6, 2H, —NCH2—), 2.89 (s, 3H, —N—CH3), 2.27 (s, 6H, Ar(CH3)2), 1.54 (br, 2H, —NCH2CH2—), 1.30 (br, 8H, —(CH2)4CH3), 0.89 (br t, J=6.6, 3 H, —CH3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06268513B1
出典データセットuspto-grants-2001_07
ORD IDord-d754c5f64d364befb0237a6127282d32
出典メモuspto-grants-2001_07