Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Phthalic Acid | HCID 1017 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Aniline | HCID 6115 | — |
| Product | Phthalic Anhydride | HCID 6811 | — |
Reaction Steps
Decarboxylation is not always a predictable reaction. For example, A. S. Sultanov, J. Gen. Chem. (USSR) 16 1835 (1946) as abstracted in CA 41:6223(e) discloses that salicylic acid may be decarboxylated by autoclaving the acid in the presence of copper bronze and benzene at 170° C. The acid alone decarboxylates at 205° C., while in the presence of aniline decarboxylation begins at 170° C. In the case of salicylic acid, aniline and copper bronze seem to be equal in catalytic ability. On the other hand, when phthalic acid is heated in aniline at 180° C., decarboxylation does not occur and instead phthalic anhydride is produced. Heating phthalic anhydride with copper bronze in chloroform at 180° C. gave a 22% yield of benzoic acid. Phthalic acid was found to decarboxylate to yield benzoic acid merely by heating in water at 235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USH0000992 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-67892ae0c9894d7f867aa008903cb3ff |
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| Source note | uspto-grants-1991_11 |
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