HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Methyl-1-naphthol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 1-Naphthol methanol | HCID 20473511 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methyl-1-naphthol | HCID 24055 | — |
| Product | 4-Methyl-1-naphthol | HCID 82483 | — |
Reaction Steps
Tasaka et al (JP 50047958) disclose the following reaction scheme: methylation of alpha-naphthol at position 2 was effected by vapor phase methylation of 1-naphthol at elevated temperature in the presence of catalyst comprising CeO2 and Sb2O3, GeO2, SnO2 or MgO. Aqueous ammonia (28%) was added to a mixture of SnCl4 and Ce(NO3)4 -2NH4NO3 2H2O in water at 50° C. The resulting precipitate was dried, calcinated for 3 hours at 600° C., and crushed to form a catalyst. 1-Naphthol/methanol mixture (1:6 molar) was passed over the catalyst at 425° C. and 1000 hr-1 space velocity to give 72.5 wt. % 2-methyl-1-naphthol, 2.6 wt. % 4-methyl-naphthol and 2.2 wt. % of other material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420362 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-89bed5156d854d7e8a8bbca45f753b6d |
| Source note | uspto-grants-1995_05 |