반응 #548580

ord-9c7841d5250b4b158d7b59a13727c286

반응 방정식

c1ccc2ccccc2c1
napthalene
O=C(O)CCC(=O)O
succinic acid
O=C(O)c1ccccc1C(=O)O
phthalic acid
O=C(O)/C=C\C(=O)O
maleic acid
O=C1C=CC(=O)c2ccccc21
napthoquinone
O=C1C=CC(=O)c2ccccc21
napthoquinone
O=C1OC(=O)c2ccccc21
phthalic anhydride
수율 99.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The optimum yield of phthalic anyhdride is produced in the temperature range of 360° ± 10° C, with temperatures over or under this range
  2. 2
    기타resulting in over or under oxidation

실험 절차

The optimum yield of phthalic anyhdride is produced in the temperature range of 360° ± 10° C, with temperatures over or under this range resulting in over or under oxidation, respectively, of the napthalene yielding undesirable products such as 1-4 napthoquinone, phthalic acid, maleic acid, succinic acid, etc. With a vanadium pentoxide catalyst structure made according to the present invention, a yield of 99% phthalic anhydride was obtained with only a slight trace of 1-4 napthoquinone. Throughout this reaction, the temperature of the catalyst structure was easily maintainable within the optimum operating temperature range of 360° C ± 10° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04062872uspto-grants-1977_12