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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107832Generated: October 31, 2026

Acetic Anhydride → HCID 14848179, compound

https://huagongshe.com/reaction/2107832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium BromideHCID 25514—
ReactantHCID 13609265HCID 13609265—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
CatalystManganese acetate tetrahydrateHCID 93021—
SolventAcetic AcidHCID 176—
ProductHCID 14848179HCID 14848179—

Reaction Conditions

Temperature120 °C

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 The vessel was cooled, and the contents were withdrawn and analyzed.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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935537
Source datasetuspto-grants-1990_06
ORD IDord-9c5638bea26245ff92f20cc3ad07e401
Source noteuspto-grants-1990_06