HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228730Generated: October 30, 2026
Hydrochloric Acid → HCID 13628209, compound
https://huagongshe.com/reaction/228730
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-Hydroxy-2-naphthoic acid | HCID 7104 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Product | HCID 13628209 | HCID 13628209 | 11% |
Reaction Steps
Dichloromethane (304 ml) and thionyl chloride (76 ml) were added to 3-hydroxynaphthalene-2-carboxylic acid (5 g), and the mixture was stirred under reflux for 4 hr. The solvent was then removed by distillation under the reduced pressure. Dioxane (200 ml) was added to the residue to prepare a solution. A solution of O,N-dimethylhydroxylamine hydrochloride (7.8 g) in a 2 N aqueous sodium hydroxide solution was added thereto, and the mixture was stirred at room temperature for one hr. Under ice cooling, the reaction solution was acidified by the addition of 4 N hydrochloric acid, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with an aqueous potassium carbonate solution and water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure to give 3-hydroxynaphthalene-2-carboxylic acid methoxymethylamide (660 mg, yield 11%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-a92cd2818f1b49738563b897543b6221 |
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| Source note | uspto-grants-2009_07 |
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