HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → trans-1,2,3,4-Tetrahydro-4-methoxy-1-naphthylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | trans-N-(1,2,3,4-tetrahydro-4-methoxy-1-naphthyl)acetamide | HCID 70617063 | — |
| Solvent | Water | HCID 962 | — |
| Product | trans-1,2,3,4-Tetrahydro-4-methoxy-1-naphthylamine | HCID 70617223 | — |
Reaction Steps
A mixture of 6.9 g. of cis and trans-N-(1,2,3,4-tetrahydro-4-methoxy-1-naphthyl)acetamide, 56.11 g. of potassium hydroxide, 50 ml. of ethylene glycol and 20 ml. of water is stirred and heated at reflux for an overnight period. The mixture is cooled, 100 ml. of water is added and the mixture extracted with methylene chloride (3 × 50 ml.). The combined extract was washed with 125 ml. of 10% sodium hydroxide solution, dried and evaporated in vacuo to afford 5.7 g. of title product - an oil. This oily amine is used without further purification for the preparation of the urea derivative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04089976 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-803ae11c6eba462ea04c80813ae580f8 |
| Source note | uspto-grants-1978_05 |