HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → (4-Chloro-phenyl)-phenylamino-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | alpha-Bromo-4-chlorophenylacetic acid | HCID 10490868 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (4-Chloro-phenyl)-phenylamino-acetic acid | HCID 2757838 | 99.8% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
2-Bromo-2-(4-chlorophenyl)acetic acid (1.2 g, 4.67 mmol) and aniline (0.85 mL, 9.33 mmol) are dissolved in acetonitrile (29 mL). The reaction is heated under microwave irradiation at 100° C. for 5 minutes. The solvent is evaporated and the residue is dissolved in EtOAc and washed with 3M HCl and then brine. The organic layer is dried over Na2SO4, filtered and evaporated to dryness to give intermediate I258 as a white solid (1.22 g, quantitative yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08835682B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-b5b9b1b80fe0497e81a29222e9861894 |
| Source note | uspto-grants-2014_09 |