4-Methylbenzoyl Chloride → N-(2-(Furan-2-yl)-2-oxoethyl)-4-methylbenzamide

反応式

Cl.[O:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7]([CH2:9][NH2:10])=[O:8].C(=O)(O)[O-].[Na+].[CH3:16][C:17]1[CH:25]=[CH:24][C:20]([C:21](Cl)=[O:22])=[CH:19][CH:18]=1>>[CH3:16][C:17]1[CH:25]=[CH:24][C:20]([C:21]([NH:10][CH2:9][C:7]([C:3]2[O:2][CH:6]=[CH:5][CH:4]=2)=[O:8])=[O:22])=[CH:19][CH:18]=1

参加物

反応物 3

HCID 134054-Methylbenzoyl Chloride

HCID 516892Sodium Bicarbonate

HCID 132261382-Amino-1-(furan-2-yl)ethan-1-one hydrochloride

生成物 1

HCID 13773124N-(2-(Furan-2-yl)-2-oxoethyl)-4-methylbenzamide収率 83.3%

実験手順

8.0 g of (2-furylcarbonyl)methylamine hydrochloride, 10.5 g of sodium bicarbonate and 9.2 g of 4-methylbenzoyl chloride are treated in the same manner as described in Preparation 1-(1). 10.0 g of N-(4-methylbenzoyl)-(2-furylcarbonyl)methylamine are thereby obtained. Yield: 83.3%