HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Acetyltetralin → HCID 240448, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Acetyltetralin | HCID 69885 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 240448 | HCID 240448 | 70.1% |
Reaction Steps
To a solution of 6-acetyltetralin (5.0 g, 29 mmol) in methanol (30 mL) under a nitrogen atmosphere was added hydroxylamine hydrochloride (2.18 g, 32 mmol) and sodium acetate (2.59 g, 32 mmol) and the resulting mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure and the residue was taken up in diethyl ether and washed with water and then with saturated sodium chloride solution. The organic phase was dried (MgSO4) and concentrated under reduced pressure to afford an oil which solidified. The solid was pulverized and rinsed with hexanes to afford the title compound of Step C (3.85 g) as an off-white solid. 1H NMR (CDCl3): δ 9.1 (br s,1H), 7.33 (m,2H), 7.07 (d,1H), 2.78 (m,4H), 2.27 (s,3H), 1.79 (m,4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962436 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-d75298fa066e4607a4de1e42c47a1021 |
| Source note | uspto-grants-1999_10 |