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HRID 2103084作成日:2026年10月26日

Dicyclohexylcarbodiimide → 2-cyclobutylidene-N-(4-methoxy-2,3-dimethylphenyl)acetamide

https://huagongshe.com/reaction/2103084

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物4-Methoxy-2,3-dimethylanilineHCID 11094809—
反応物2-Cyclobutylideneacetic acidHCID 21923173—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物2-cyclobutylidene-N-(4-methoxy-2,3-dimethylphenyl)acetamideHCID 6905332765.3%

反応手順

Cyclobutylideneacetic acid (3.8 g), 5,6-dimethyl-4-methoxyaniline (5 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDC) (4.7 g), 1,3-dicyclohexylcarbodiimide (DCC) (2.4 g), 4-dimethylaminopyridine (DMAP) (805 mg) and triethylamine (TEA) (7.3 g) were dissolved in dichloromethane (80 mL). The mixture was stirred at room temperature overnight, concentrated, and the residue dissolved in ethyl acetate. The organic phase was washed with water (3×20 mL) and 1M HCl (3×20 mL), and a white solid was filtered out. The organic solution was then dried out by evaporation giving 2-cyclobutylidene-N-(4-methoxy-2,3-dimethylphenyl)acetamide as a brown solid (5.3 g). The product was used in the next step without further purification. MS: (m/z)=246 (100, M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07576094B2
出典データセットuspto-grants-2009_08
ORD IDord-e76f5d88b4074044a32e6ad90da2d763
出典メモuspto-grants-2009_08