HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl Bromide → 6-Bromo-1-ethyl-3,4-dihydroquinolin-2(1H)-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl Bromide | HCID 6332 | — |
| Edukt | 6-Bromo-3,4-dihydroquinolin-2(1H)-one | HCID 14373281 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 6-Bromo-1-ethyl-3,4-dihydroquinolin-2(1H)-one | HCID 66911304 | 69% |
Reaktionsschritte
To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (750 mg, 3.32 mmol) in 20 ml dry DMF was added potassium tert-butylate (804 mg, 6.64 mmol). After the mixture was stirred for 30 min at room temperature, a solution of ethyl bromide (724 mg, 6.64 mmol) in 10 ml dry DMF was added. Following overnight stirring, the mixture was diluted with 150 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, 1/1, Rf=0.52) gave 6-bromo-1-ethyl-3,4-dihydro-1H-quinolin-2-one (583 mg, 2.29 mmol, 59%) as a colorless solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08541404B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-1ce98bb2e7c3438e8b24f96ce768f4f9 |
| Quellennotiz | uspto-grants-2013_09 |