HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429782Generated: October 30, 2026
Hydrochloric Acid → HCID 9914839, compound
https://huagongshe.com/reaction/429782
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 18007941 | HCID 18007941 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 9914839 | HCID 9914839 | — |
Reaction Steps
In a 100 ml round-bottomed flask containing 30 ml of methanol, add sodium (0.07 g 0.0030 at. g.) in small portions. When the sodium has been completely used up, add naphthol (0.82 g, 3.6 mmol). Stir using a magnetic stirrer for 20 minutes. Remove the methanol by evaporation under reduced pressure. Take up the resulting residue in 15 ml of dimethylformamide. Add the compound obtained in Step C (1.2 g, 3 mmol) and heat at reflux for 12 hours. Allow the reaction mixture to cool and pour it into a mixture of 100 ml of water and 10 ml of 3M hydrochloric acid. Extract the aqueous phase twice with ethyl acetate. Wash the organic phase with an aqueous 10% sodium hydroxide solution and then with water. Dry over magnesium sulphate and remove the ethyl acetate by evaporation under reduced pressure. Recrystallise the resulting solid residue from acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06319930B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-4159b4c7d2ba4ed882bef400adcefc1d |
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| Source note | uspto-grants-2001_11 |
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