HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-bromo-2-fluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Bromo-2-fluorobenzoic acid | HCID 2736313 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 3-bromo-2-fluorobenzoate | HCID 17832538 | 92% |
Reaction Steps
To a stirred solution of 3-bromo-2-fluorobenzoic acid 1 (25.0 g, 114.15 mmol) in ethanol (400 mL) was added conc. H2SO4 (3 mL) at RT and stirred at reflux temperature for 24 h. The reaction was monitored by LC-MS; after completion of the reaction, the reaction mixture was concentrated to obtain the residue. The residue was diluted with EtOAc (500 mL), washed with water (300 mL), brine (300 mL), dried over Na2SO4, filtered and concentrated under reduced pressure to afford compound 2 (26.0 g, 92%) as a light yellow liquid. 1H NMR (400 MHz, CDCl3): δ 7.88-7.84 (m, 1H), 7.72-7.69 (m, 1H), 7.08-7.04 (m, 1H), 4.39 (q, J=7.2 Hz, 2H), 1.39 (t, J=7.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09334261B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-539e6fae1a124264825c4df4093d9d0b |
| Source note | uspto-grants-2016_05 |