HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → Ethyl 4-Amino-2-fluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 4-Acetamido-2-fluorobenzoic acid | HCID 13041370 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-Amino-2-fluorobenzoate | HCID 10797532 | — |
Reaction Steps
A solution of 10.0 g of 4-acetamido-2-fluorobenzoic acid, 100 ml of ethyl alcohol and 2.0 ml of boron trifluoride etherate is heated under reflux for 22 hours. The solvent is slowly removed by distillation as an equal amount of fresh ethyl alcohol is added. After 200 ml of solvent has been removed, the remainder is evaporated at reduced pressure. The residue is dissolved in ethyl acetate, washed with saturated aqueous sodium bicarbonate, dried and the solvent then evaporated to yield a solid. Recrystallization of the solid from ethanol-hexane yields ethyl 4-amino-2-fluorobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04333940 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-b7df3b592cee4ad9a707e91fb97d8101 |
| Source note | uspto-grants-1982_06 |