HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 6-Bromo-3,4-dihydroquinolin-2(1H)-one | HCID 14373281 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-one | HCID 63106141 | 78% |
Reaction Steps
To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (339 mg, 1.50 mmol) in 15 ml dry DMF was added potassium tert-butylate (336 mg, 3.0 mmol). After the mixture was stirred for 30 min at room temperature, a solution of methyl iodide (426 mg, 3.0 mmol) in 5 ml dry DMF was added. Following overnight stirring, the mixture was diluted with 100 ml 1 N HCl. Extraction with ethyl acetate (2×100 mL) followed by washing of the organic extracts with water and brine, drying over MgSO4 and removal of the solvent in vacuo gave a light yellow solid. Purification by flash chromatography (hexanes/ethyl acetate, 7/3, Rf=0.21) gave 6-bromo-1-methyl-3,4-dihydro-1H-quinolin-2-one (281 mg, 1.17 mmol, 78%) as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08685960B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-07a10a81436f41939437260f955e2692 |
| Source note | uspto-grants-2014_04 |