HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-(2-dimethylamino-ethoxy)-3,4-dihydro-2H-naphthalen-1-one Oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 6-(2-Dimethylaminoethoxy)-1-tetralone | HCID 12214387 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-(2-dimethylamino-ethoxy)-3,4-dihydro-2H-naphthalen-1-one Oxime | HCID 72440628 | — |
Reaction Steps
A solution of 6-(2-dimethylamino-ethoxy)-3,4-dihydro-2H-naphthalen-1-one (0.53 g, 2.3 mmol), hydroxylamine hydrochloride (Riedel DeHaen, 0.69 g, 10.0 mmol), and Et3N (Aldrich, 1.4 mL, 10.0 mmol) in MeOH (6 mL) was heated to reflux overnight. The reaction mixture was diluted with EtOAc (70 mL) and washed with 10% Na2CO3, brine. The organic solution was dried over Na2SO4, filtered and concentrated in vacuo to afford the product as an off-white solid. MS (ESI): 249 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425631B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-ea227f3f465f4bc0a9880d52e033bbaf |
| Source note | uspto-grants-2008_09 |