3-[2-(Acetyloxy)ethyl]dihydro-2(3H)-furanone → 2H-Pyran-4-carboxylic acid, tetrahydro-, methyl ester

反応式

[C:1]([O:4][CH2:5][CH2:6][CH:7]1[CH2:11][CH2:10][O:9][C:8]1=[O:12])(=O)C.COCCC1CCOC1=O>[O-2].[Al+3].[O-2].[O-2].[Al+3].CO>[O:4]1[CH2:1][CH2:11][CH:7]([C:8]([O:9][CH3:10])=[O:12])[CH2:6][CH2:5]1

参加物

実験手順

A solution consisting of 37 wt % of 3-(2'-acetoxyethyl)-dihydro-2(3H)furanone, 19 wt % of 3-(2'-methoxyethyl)dihydro-2(3H)furanone, and 44 wt % of methanol, was passed over 140 g of aluminum oxide catalyst (1.5 mm extrudates) in a tubular reactor at a rate of 38 g per hour with the addition of 10 Lh of nitrogen, at a temperature of 250° C. The gaseous effluent was condensed in cold traps and analyzed by gas chromatography. 53 mol % of methyl tetrahydropyran-4-carboxylate was formed, plus 41 mol % of 3-(2'-methoxyethyl)-dihydro-2(3H)furanone and 3 mol % of 5-oxaspiro[2.4 ]heptan-2-one. The conversion of 3-(2'-acetoxyethyl)-dihydro-2(3H)furanone was better than 99%.