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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107833Generated: October 31, 2026

6-(Acetyloxy)-2-naphthalenecarboxylic acid → HCID 14848179, compound

https://huagongshe.com/reaction/2107833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Acetyloxy)-2-naphthalenecarboxylic acidHCID 87038—
ReactantHCID 13609265HCID 13609265—
ProductHCID 14848179HCID 14848179—

Reaction Steps

The 2-methyl-6-acetyloxynaphthalene obtained in the first half of Example 1 was not recrystallized from acetic anhydride prior to oxidation, but was directly oxidized with molecular oxygen in the presence of the same catalyst as in Example 1 in the same reactor as in Example 1. The reaction time was 2.4 hours. After the reaction, the product was analyzed. The conversion of 2-methyl-6-acetyloxynaphthalene was 55.5 mole %, and the yield of 6-acetyloxy-2-naphthoic acid was 40.0 mole % (selectivity 72 mole %). At this time, 8.88 mole % of 6-acetyloxy-2-naphthaldehyde was formed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935537
Source datasetuspto-grants-1990_06
ORD IDord-d1c15946363841bf9c159ef00ba42a6f
Source noteuspto-grants-1990_06