HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoro-N-methylaniline → Ethyl 2-((4-fluorophenyl)(methyl)amino)-2-phenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoro-N-methylaniline | HCID 68024 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl bromophenylacetate | HCID 97780 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 2-((4-fluorophenyl)(methyl)amino)-2-phenylacetate | HCID 58556946 | 100% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
4-Fluoro-N-methylaniline (0.33 g, 2.67 mmol) is added to a solution of ethyl 2-bromo-2-phenylacetate (0.36 mL, 2.06 mmol) in acetonitrile (6.86 mL) and DIPEA (0.47 ml, 2.67 mmol). The dark solution is stirred at 100° C. under microwave irradiation for 1 hour. Then solvent is evaporated and the crude is purified by flash chromatography (Petroleum ether/EtOAc=97/3) to obtain intermediate I118 as a yellow solid (0.59 g, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455646B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-410993a3413e478bae35e461e1cc8091 |
| Source note | uspto-grants-2013_06 |