HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234578Generated: November 3, 2026
Hydrochloric Acid → 6-(Acetyloxy)-2-naphthalenecarboxylic acid
https://huagongshe.com/reaction/234578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Hydroxy-2-naphthoic acid | HCID 85557 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(Acetyloxy)-2-naphthalenecarboxylic acid | HCID 87038 | 74.8% |
Reaction Steps
In a 100 ml-reaction vessel, 16.7 g (2.53×10-1M) of potassium hydroxide and 85 ml of water were placed, followed by cooling to 0° C. To the mixture, 20.0 g (1.06×10-1M) of 6-hydroxy-2-naphthoic acid was added and dissolved therein. To the solution, 10.9 g (1.07×10-1M) of acetic anhydride was added dropwise in 40 minutes at 0° C. followed by stirring for 2 hours. After stirring, the reaction mixture was acidified with 6N-hydrochloric acid to precipitate a crystal. The crystal was recovered by filtration, followed by washing with water and drying to obtain 18.3 g of 6-acetoxy-2-naphthoic acid (Yield: 74.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05595685 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-813f9efe0a874d70ae996de60db0c895 |
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| Source note | uspto-grants-1997_01 |
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