HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 2-(4-Bromophenyl)-N-{2-(3-methoxyphenyl)ethyl}-N-phenylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Benzeneacetyl chloride, 4-bromo- | HCID 181552 | — |
| Reactant | Bromophenylacetyl chloride | HCID 598182 | — |
| Reactant | HCID 13467414 | HCID 13467414 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Bromophenyl)-N-{2-(3-methoxyphenyl)ethyl}-N-phenylacetamide | HCID 23440798 | 98% |
Reaction Steps
To a solution of {2-(3-methoxyphenyl)ethyl}phenylamine (1.06 g, 4.65 mmol) in ethyl acetate (80 mL) under nitrogen was added a solution of 4-bromophenylacetyl chloride (1.06 g, 4.65 mmol) in ethyl acetate (20 mL), the bromophenylacetyl chloride being prepared from the corresponding carboxylic acid (1 g, 4.65 mmol) and oxalyl chloride (0.61 mL, 6.98 mmol) in CH2Cl2 (20 mL). After 1 hour, the reaction was poured into water (50 mL). The organic layer was dried over MgSO4, filtered and concentrated to provide the title compound (1.92 g, 98% yield): EI-MS (m/z) 423.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436923B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-a85addbaf17242838219bb318010e1da |
| Source note | uspto-grants-2002_08 |