HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → N,N-dimethyl-5-methoxy-2-bromophenylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 5-Methoxy-2-bromophenylacetyl chloride | HCID 18451529 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N,N-dimethyl-5-methoxy-2-bromophenylacetamide | HCID 18451566 | — |
Reaction Steps
5-Methoxy-2-bromophenylacetyl chloride (60 g, 0.23 mol) is dissolved in anhydrous Et2O (400 mL), stirred and cooled in an ice bath. A 2 M solution of dimethylamine (228 mL, 0.46 mol) is added dropwise and the mixture allowed to warm to room temperature and stirred for 2 hours. Additional Et2O (500 mL) is added. The organic solution is washed with 1 N HCl (2×500 mL), saturated NaHCO3 (500 mL) and brine (500 mL). The organic layer is dried (Na2SO4) and concentrated by rotary evaporator. The residue is purified using flash chromatography (hexanes/EtOAc, from 7:3 to 1:9). Trituration of the crude product with Et2O/hexanes gives N,N-dimethyl-5-methoxy-2-bromophenylacetamide as a white crystalline solid (m.p. 88–90° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202364B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-004c3462ebdf41948f00335f39e12ac2 |
| Source note | uspto-grants-2007_04 |