Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | N-(7-methoxynaphthalen-1-yl)acetamide | HCID 11447230 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Acetamido-2-tetralone | HCID 13424111 | 42.8% |
Reaction Steps
Ammonia (300 mL) was condensed in a flask containing 8-Acetamido-2-methoxynaphthalene (24.5 g, 115 mmol), t-butyl alcohol (34 g, 0.46 mol) and THF (300 mL). Sodium (8 g, 0.35 mol) was added in portions and the mixture was stirred for 3 h and allowed to warm to room temperature. The mixture was poured onto ice and saturated sodium chloride, and then extracted with THF (3×). The combined organic layers were washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to give a dark solid. The residue was dissolved in 50% acetic acid and heated at 95° C. for 18 h. After evaporation, the residue was suspended in dimethyl ether and collected by filtration and dried. The filtrate was purified by silica gel chromatography (3:2 EtOAc:hexane) and combined with the other product to give a tan solid (10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05721234 |
|---|
| Source dataset | uspto-grants-1998_02 |
|---|
| ORD ID | ord-9067906bf602496ea95b8c9492f74b14 |
|---|
| Source note | uspto-grants-1998_02 |
|---|