| 摘要 |
1364526 t-Caprolactone BAYER AG 29 July 1971 [1 Aug 1970] 35732/71 Heading C2C t-Caprolactone is obtained by oxidizing cyclohexanol with molecular oxygen in the liquid phase, hydrolysing the initially formed cyclohexanone peroxide to cyclohexanone and H 2 O 2 , extracting the H 2 O 2 with H 2 O, adding to the resulting aqueous H 2 O 2 solution at least one compound of the formula removing substantially all of the H 2 O, reacting the reaction mixture with an aliphatic fatty acid or with a compound which produces an aliphatic fatty acid under the reaction conditions, optionally in the presence of an esterification catalyst, dehydrating once again, and reacting the resulting per-carboxylic acid, either unchanged, after neutralization of the esterification catalyst or after purification of the percarboxylic acid, with the cyclohexanone formed in the first stage to form t-caprolactone, wherein m, n and p are 0 or 1 provided that m, n and p are not simultaneously 0, R 1 , R 2 and R 3 represent optionally substituted straight or branched-chain C 1- C 6 alkyl or optionally substituted C 4- C 6 cycloalkyl radicals up to two of the radicals R 1 , R 2 and R 3 may represent hydrogen, one of the radicals R 1 , R 2 and R 3 may represent an optionally substituted phenyl radical, or R 1 together with R 2 may represent a C 2-7 alkylene radical. The molar ratio of H 2 O 2 to carboxylic acid is preferably in the range from 1 : 1À1 to 1 : 1À5 and a 1À5-3 molar excess of cyclohexanone is preferably used. The dehydration reactions may be effected by distillation under reduced pressure with the aid of an inert diluent. A suitable form of apparatus for continuous operation of the process is described. |
