HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,2-Dichloroethane → (4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Ethylmorpholine | HCID 7525 | — |
| Edukt | Morpholine | HCID 8083 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 4-Bromo-3-fluorobenzoic acid | HCID 2773341 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanone | HCID 48474115 | 98,5% |
Reaktionsschritte
A 500 mL flask was charged with 4-bromo-3-fluorobenzoic acid (5.00 g, 22.83 mmol), 100 mL DMF, morpholine (2.4 ml, 27.5 mmol), and 4-Ethylmorpholine (8.6 ml, 67.9 mmol). HOBt (4.32 g, 32.0 mmol) was added followed by EDC (5.25 g, 27.4 mmol) and the reaction allowed to stir at room temperature for 18 hours. The reaction was concentrated and the resulting orange syrup taken up in 100 mL EtOAc and 100 mL water. The organic layer was washed with 100 mL 2N HCl, 100 mL saturated sodium bicarbonate, and 100 mL saturated sodium chloride. The organic was then dried with MgSO4, filtered, and concentrated to give 6.476 g (98%) of a viscous yellow oil. This material was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08980890B2 |
| Quelldatensatz | uspto-grants-2015_03 |
| ORD ID | ord-cd956a24b4504c40bbfe1314efeebbc1 |
| Quellennotiz | uspto-grants-2015_03 |