HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-(4-BROMOPHENYL)-N,N-DIMETHYLETHANAMINE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(4-bromophenyl)-N,N-dimethylacetamide | HCID 4631595 | — |
| Reactant | Ether tetrahydrofuran | HCID 21868444 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-BROMOPHENYL)-N,N-DIMETHYLETHANAMINE | HCID 10751802 | 12.9% |
Reaction Steps
To a suspension of LiAlH4in ether (5 mL) was added a solution of 2-(4-bromophenyl)-N,N-dimethylacetamide (1.1 g, 4.5 mmol) in 5:1 ether/THF (12 mL), giving a small exotherm. The mixture was stirred at room temperature for 3 h, refluxed overnight then cooled to 0° C. Water (0.5 mL) was added dropwise and the mixture stirred vigourously for 3 h, then poured into 1 M NaOH and extracted with ether. The organic phase was washed with brine and dried over MgSO4. Purification by flash chromatography (4% to 8% MeOH/dichloromethane+0.5% ammonium hydroxide) provided 132 mg of 2-(4-bromophenyl)-N,N-dimethylethanamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07012075B2 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-61ea48b0fc334f87ade1929632ac5652 |
| Source note | uspto-grants-2006_03 |