HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butane → Phthalic Anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butane | HCID 7843 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 3-Methyl-3-buten-1-ol | HCID 12988 | — |
| Reactant | 3-Methyl-2-butenal | HCID 61020 | — |
| Product | Phthalic Anhydride | HCID 6811 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05484576 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-d20fddd0836f4a3da7beff7e8dc9062b |
| Source note | uspto-grants-1996_01 |