HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-(Acetyloxy)-2-naphthalenecarboxylic acid → HCID 14848179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-(Acetyloxy)-2-naphthalenecarboxylic acid | HCID 87038 | — |
| Reactant | HCID 13609265 | HCID 13609265 | — |
| Product | HCID 14848179 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04801737 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-1e80a65ba87043a6badeddc169460469 |
| Source note | uspto-grants-1989_01 |