HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 2-(4-amino-3-fluorophenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(4-Amino-3-fluorophenyl)propanoic acid | HCID 13065231 | — |
| Product | Ethyl 2-(4-amino-3-fluorophenyl)propanoate | HCID 20364696 | 87% |
Reaction Steps
To a solution of 2-(4-Amino-3-fluorophenyl)propionic acid (1 g, 5.459 mmol) in EtOH was added SOCl2 (0.6 ml, 8.189 mmol) at 0° C. The mixture was stirred for 2 hours at room temperature and then SOCl2 was removed under reduced pressure. The residue was diluted with EtOAc and washed with a saturated NaHCO3 solution. The resulting mixture was dried over MgSO4 and concentrated. The residue was purified by column chromatography to afford ethyl 2-(4-amino-3-fluorophenyl)propanoate (1 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946204B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-79ca0700f8bd465ea5f1e26d92067418 |
| Source note | uspto-grants-2015_02 |