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HRID 915359作成日:2026年10月27日

Triethylamine → 2-methyl-N-[(4-methylphenyl)methyl]benzamide

https://huagongshe.com/reaction/915359

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-MethylbenzylamineHCID 66035—
反応物2-Methylbenzoyl chlorideHCID 70276—
溶媒DichloromethaneHCID 6344—
生成物2-methyl-N-[(4-methylphenyl)methyl]benzamideHCID 83547985%

反応手順

A solution of 4-methylbenzylamine (2.0 mL, 15.7 mmol), and triethylamine (4.4 mL, 31.6 mmol) in CH2Cl2 (50 mL) was cooled in an ice bath and treated dropwise with 2-methylbenzoyl chloride (2.5 mL, 19.2 mmol). After the end of the addition the ice bath was removed and the reaction mixture was allowed to warm to ambient temperature. After stirring at ambient temperature for 14 hours the resulting white suspension was diluted with CH2Cl2 (100 mL), and quenched by the addition of water (20 mL) and saturated aqueous sodium bicarbonate (20 mL). The aqueous layer was extracted with CH2Cl2 (3×30 mL), and the combined organics were dried over Na2SO4, filtered and concentrated to afford a white solid. The crude solid was recrystallized from ethyl acetate/hexane to afford 2-methyl-N-(4-methylbenzyl)benzamide (3.18 g, 85% yield) as a white crystalline solid: 1H-NMR (400 MHz, CDCl3): δ 7.36 (1H, dd, J=7.6, 1.3 Hz), 7.32-7.14 (7H, m), 5.98 (1H, br s), 4.59 (2H, d, J=5.6 Hz), 2.47 (3H, s), 2.35 (3H, s) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07265131B2
出典データセットuspto-grants-2007_09
ORD IDord-43ec7ae019a34efc871a9eecb8d2e0f4
出典メモuspto-grants-2007_09