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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantAcenaphtheneHCID 6734—
ReactantTriethanolamineHCID 7618—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BromideHCID 253881—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
CatalystManganese acetate tetrahydrateHCID 93021—
SolventAcetic AcidHCID 176—
SolventChlorobenzeneHCID 7964—
ProductNaphthalene-1-carbonyl naphthalene-1-carboxylateHCID 35039979%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04212813
Source datasetuspto-grants-1980_07
ORD IDord-f8b6c5542e7f47b7b3d3619b5b431772
Source noteuspto-grants-1980_07