Reaction #462209

ord-d20fddd0836f4a3da7beff7e8dc9062b

Reaction equation

O=C1C=CC(=O)O1
maleic anhydride
C=C(C)CCO
3-methyl-3-buten-1-ol
CCCC
n-butane
CC(C)=CC=O
3-methyl-2-buten-1-al
O=C1OC(=O)c2ccccc21
phthalic anhydride

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

Examples of reactions which can be carried out particularly expediently in the reactors according to the invention are, without this listing being exhaustive: dehydrogenations, for example, of cyclohexylidene-aniline to give diphenylamine and of cyclohexenyl-cyclohexanone to give o-phenylphenol; hydrogenations, for example, of nitrobenzene to give aniline and of phenol to give cyclohexanone; oxidative alcohol dehydrogenations, for example, of 3-methyl-3-buten-1-ol to give 3-methyl-2-buten-1-al; selective oxidations of hydrocarbons, for example, of n-butane to give maleic anhydride, of oxylene to give phthalic anhydride and of propene to give acrolein or acrylic acid and alkylations and halogenations.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05484576uspto-grants-1996_01