HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-Naphthol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Naphthalenol, potassium salt (1:1) | HCID 23672323 | — |
| Product | 1-Naphthol | HCID 7005 | — |
Reaction Steps
An alcoholic solution of potassium α-naphtholate produced as in Example 4 hereinabove is acidified with gaseous hydrochloric acid taken in the equimolar amount relative to potassium α-naphtholate at a temperature ranging from 20° to 30° C. After separation of precipitated pure potassium chloride, the solution of α-naphthol in ethanol is separated following the procedure described in the foregoing Example 4 to give 116 g of α-naphthol with a purity of 97.5%. The total yield of α-naphthol is 140 g (98% of theory) as calculated for the employed naphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04237323 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-912bef2c42d74b9d93a8c050feef8d2b |
| Source note | uspto-grants-1980_12 |