HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 6-(Acetyloxy)-2-naphthalenecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-Hydroxy-2-naphthoic acid | HCID 85557 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(Acetyloxy)-2-naphthalenecarboxylic acid | HCID 87038 | 99% |
Reaction Steps
25 Grams (133 mmol) of 6-hydroxy-2-naphthoic acid and 68 g (265 mmol) of acetic anhydride were placed in a reactor, and while the mixture was stirred, 0.05 g of concentrated sulfuric acid was added. The mixture was stirred until heat generation ceased, and the mixture was further heated and stirred at 80° C. for 1 hour and then gradually cooled to room temperature. While the reaction mixture was cooled in an ice bath, 500 g of water was gradually added, and the mixture was stirred at room temperature for 3 hours to quench unreacted acetic anhydride. A precipitated white solid was recovered by filtration, washed with water to remove acetic acid, and dried with a vacuum dryer, to give 30.3 g of an end compound (yield 99%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06730371B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-f97836bbd0c64e2c8d8e207653046f63 |
| Source note | uspto-grants-2004_05 |