反応 #346879

ord-7e1b3307ac0846ff897be254a16843b3

反応方程式

COC(OC)N(C)C
N,N-dimethylformamide dimethyl acetal
CCC(=O)N(C)C
N,N-dimethylpropionamide
FC1(F)Oc2ccccc2O1
2,2-difluoro-1,3-benzodioxole
CC(=O)Cc1cccc2c1OC(F)(F)O2
1-(2,2-difluoro-1,3-benzodioxol-4-yl)propanone

反応条件

温度
70°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他obtained

実験手順

12 g of 1-(2,2-difluoro-1,3-benzodioxol-4-yl)propanone are prepared by condensation of N,N-dimethylpropionamide with the lithiated anion of 2,2-difluoro-1,3-benzodioxole obtained according to the procedure described in patent EP 333658, are then dissolved in 14.6 ml (0.11 mol) of N,N-dimethylformamide dimethyl acetal and heated at 70° C. according to the procedure described in Example No. 1. 25 g (0.05 mol) of enaminone thus obtained are dissolved in 130 ml of acetic acid and then 3.3 ml (0.069 mol) of hydrazine hydrate are added. The crude product obtained is purified by trituration in pentane.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05523280uspto-grants-1996_06