Dimethylformamide → 2-(5-methyl-1H-imidazol-4-yl)ethanol oxalate

反応式

Br[CH:2]1[CH2:6][CH2:5][O:4][C:3]1([CH3:8])[OH:7].C(O)(=[O:11])C.[CH:13]([NH2:15])=[NH:14].C(NCC)C.CN(C)[CH:23]=[O:24]>>[C:23]([OH:24])(=[O:11])[C:3]([OH:7])=[O:4].[CH3:8][C:3]1[NH:15][CH:13]=[N:14][C:2]=1[CH2:6][CH2:5][OH:4]

参加物

反応物 4

HCID 6228Dimethylformamide

HCID 8021Diethylamine

HCID 160693Formamidine acetate

HCID 212994013-Bromo-2-methyl-tetrahydrofuran-2-ol

生成物 1

HCID 212994002-(5-methyl-1H-imidazol-4-yl)ethanol oxalate収率 42%

反応条件

温度: 80 °C

実験手順

5.0 g of 3-bromo-2-methyl-tetrahydrofuran-2-ol and 5.75 g of formamidine acetate were added to 15 ml of N,N-dimethylformamide. 5 g of diethylamine was slowly added to the reaction mixture, which was then stirred for about 4 hours at 80° C. and was distilled in vacuo for about 1 hour at the same temperature. The resulting oily residue was diluted with 25 ml of acetone. 4.95 g of oxalic acid was added to the reaction mixture, which was then stirred for about 1 hour. The resulting solid was filtered and washed with acetone to give 2.5 g of 2-(5-methyl-1H-imidazol-4-yl)ethanol oxalate (yield: 42%).