Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ammonium Bromide | HCID 25514 | — |
| Reactant | HCID 13609265 | HCID 13609265 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Catalyst | Manganese acetate tetrahydrate | HCID 93021 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 14848179 | HCID 14848179 | — |
Reaction Steps
A 200 cc titanium pressure vessel equipped with a stirrer was charged with 10 parts of 2-methyl-6-acetyloxynaphthalene, 80 parts of acetic acid, 20 parts of acetic anhydride, 0.249 parts (Co=590 wt. ppm) of cobalt acetate tetrahydrate, 0.245 parts (Mn=550 wt. ppm) of manganese acetate tetrahydrate, and 0.250 parts (Br=2040 wt. ppm) of ammonium bromide. The vessel was pressurized with air to 25 kg/cm2 -G, and the mixture was heated to 120° C. Air was introduced into the vessel at a rate of 10 Nl/hr. When the absorption of oxygen ceased, the reaction was terminated. The reaction time was 2.5 hours. The vessel was cooled, and the contents were withdrawn and analyzed. The conversion of 2-methyl-6-acetyloxynaphthalene was 100 mole %, and the yield of 6-acetyloxy-2-naphthoic acid was 68.5 mole % (selectivity 68.5 mole %). At this time, 23.5 mole % of 6-acetyloxy-2-naphthaldehyde was also formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04935537 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-9c5638bea26245ff92f20cc3ad07e401 |
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| Source note | uspto-grants-1990_06 |
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