HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 45074003 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one | HCID 58318043 | — |
Reaction Steps
A mixture containing 5-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (1 g, 4 mmol), chloroacetone (407 mg, 4.4 mmol) and potassium carbonate (1.38 g, 10 mmol) in dimethyl formamide (DMF) (8 ml) is stirred at room temperature for 18 hours. To this mixture is added water (50 ml) and ethyl acetate (50 ml). The organic layer is separated, washed with brine, dried over MgSO4, and concentrated. The crude product is purified by flash column chromatography using 30% ethyl acetate in dichloromethane as eluent to give 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one as an orange oil. LC-MS m/z: 269.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216964B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-fa029e8b621649dc8a8aca503df3aa64 |
| Source note | uspto-grants-2015_12 |