Dimethylformamide dimethyl acetal → N-[1-Dimethylaminomethylidene]-3-methylsulfanylbenzamide
反応式
[CH3:1][S:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[C:6]([NH2:8])=[O:7].CO[CH:14](OC)[N:15]([CH3:17])[CH3:16]>CO>[CH3:14][N:15]([CH3:17])[CH:16]=[N:8][C:6](=[O:7])[C:5]1[CH:9]=[CH:10][CH:11]=[C:3]([S:2][CH3:1])[CH:4]=1参加物
4
実験手順
8.5 g of 3-methylsulfanylbenzamide and 18 ml of dimethylformamide dimethyl acetal were heated at 120° C. while the formed methanol was eliminated by distillation. After heating for 3 h, the volatiles were removed in vacuo. The crude product was purified by flash chromatography (300 g silica gel; DCM/MOH, gradient from 100:0 to 95:5). 8 g of the title compound were obtained as an oil.
後処理
- distillationwas eliminated by distillation
- temperatureAfter heating for 3 h
- customthe volatiles were removed in vacuo
- customThe crude product was purified by flash chromatography (300 g silica gel; DCM/MOH, gradient from 100:0 to 95:5)
出典と根拠
- ORDレコード
- ord-af8e0a68413e4818b933fa093ce5b3de
- 出典データセット
- uspto-grants-2011_12
- 特許番号
- US08076324B2
反応ノート
読み込み中…