Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Chlorotoluene | HCID 7238 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Catalyst | Sodium Bromide | HCID 253881 | — |
| Product | 2-Chlorobenzoic Acid | HCID 8374 | 85.8% |
Reaction Steps
Analogously to Example 1, 300 g of o-chlorotoluene was oxidized in the presence of 100 g of acetic acid, 3 g of cobalt acetate tetrahydrate and 1.5 g of sodium bromide at a pressure of 25 bar, a temperature of 110°-130° C., and a gas exhaust rate of 3 1/min. After the oxidation had ended, 450 g of 50% acetic acid was added, the mixture was cooled to 25° C. and filtered, and the filter cake was washed with 750 g of 50% acetic acid, the mother liquor (314.5 g) and washing filtrates (693.5 g) being recovered separately. The dried filter cake yielded 318.5 g of o-chlorobenzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04603220 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-88d12c21a8bd4069be1f5b712d78708b |
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| Source note | uspto-grants-1986_07 |
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