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HRID 1487025作成日:2026年10月27日

Isobutylamine → 2,4-dimethyl-N-(2-methylpropyl)aniline

https://huagongshe.com/reaction/1487025

反応式

関与物質

役割名称HCID仕込み量
反応物IsobutylamineHCID 6558—
反応物TetrahydrofuranHCID 8028—
反応物1-Chloro-2,4-dimethylbenzeneHCID 523153—
生成物2,4-dimethyl-N-(2-methylpropyl)anilineHCID 2842238996.3%

反応条件

温度70 °C

反応手順

A mixture of 1-chloro-2,4-dimethylbenzene (1687 mg, 12 mmol), isobutylamine (1755 mg, 24.00 mmol), and Caddick catalyst (140 mg, 0.238 mmol) was treated with lithium hexamethyl disilizide in tetrahydrofuran (1 M LHMDS in THF, 15 mL, 15.00 mmol) under nitrogen. The reaction mixture was heated to 70° C. for 45 minutes in a septum-sealed vessel. The cooled mixture was concentrated in vacuo and the residue was partitioned between aqueous citric acid (50 mL) and tert butyl methyl ether (TBME) (2×50 mL). The organic phase was treated with dried MgSO4, the solid removed by filtration and the organic phase was concentrated in vacuo to give (2,4-dimethylphenyl)(2-methylpropyl)amine (2.05 g, 11.56 mmol) as an orange oil. LCMS [LCMS1] Rt 1.03 min, m/z (ES+) 178 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09428452B2
出典データセットuspto-grants-2016_08
ORD IDord-c561e36556e34bc0ab77e7f6e38f36d6
出典メモuspto-grants-2016_08