HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-(3-methoxy-2-hydroxypropyl)-6-benzyloxy-2-naphthylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(6-Benzyloxy-2-naphthyl)-5-methoxymethyl-2-oxazolidone | HCID 131717725 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(3-methoxy-2-hydroxypropyl)-6-benzyloxy-2-naphthylamine | HCID 19012494 | 88.1% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of 2.0 g of 3-(6-benzyloxy-2-naphthyl)-5-methoxymethyl-2-oxazolidone, 20 ml of ethanol, 4 ml of water and 1.08 g of potassium hydroxide is stirred at 100° C. for one hour. The reaction mixture is evaporated under reduced pressure to remove the ethanol. The residue is extracted with ethyl acetate, and the extract is washed with water, dried and evaporated under reduced pressure to remove the solvent. The residue is recrystallized from ethyl acetate - hexane to give 1.64 g of N-(3-methoxy-2-hydroxypropyl)-6-benzyloxy-2-naphthylamine as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05332754 |
| Source dataset | uspto-grants-1994_07 |
| ORD ID | ord-7c269d4b45724c90aa48e5eef4302e18 |
| Source note | uspto-grants-1994_07 |