HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057721Generated: October 26, 2026
Oxygen → Naphthalene-1-carbonyl naphthalene-1-carboxylate
https://huagongshe.com/reaction/2057721
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Acenaphthene | HCID 6734 | — |
| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Catalyst | Manganese acetate tetrahydrate | HCID 93021 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | Naphthalene-1-carbonyl naphthalene-1-carboxylate | HCID 350399 | 79% |
Reaction Steps
8 g of acenaphthene, 0.45 g of cobalt acetate tetrahydrate, 0.045 g of manganese acetate tetrahydrate, 0.045 g of NaBr, 0.17 ml of triethanolamine, 30 ml of acetic acid, and 50 ml of chlorobenzene were charged in the same manner as in Example 1. The air in the system was substituted with oxygen gas and the system was heated to 65° C., the reaction setting in. Acetic anhydride was dropped while gradually heating the reaction system for reaction. The reaction was continued for 42 hours during which the reaction temperature was increased up to 90° C. The total amount of absorbed oxygen reached 3170 ml and acetic anhydride was added in an amount of 7 ml. After completion of the reaction, the reaction mixture was cooled to allow crystals to precipitate and the crystals were separated by filtration, washed with water and dried to obtain 8.1 g of yellowish white naphthalic anhydride (yield 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04212813 |
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| Source dataset | uspto-grants-1980_07 |
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| ORD ID | ord-f8b6c5542e7f47b7b3d3619b5b431772 |
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| Source note | uspto-grants-1980_07 |
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