HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239461Generated: October 28, 2026
Methanol → Methyl 5-amino-2-fluorobenzoate
https://huagongshe.com/reaction/239461
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Amino-2-fluorobenzoic acid | HCID 2735910 | — |
| Product | Methyl 5-amino-2-fluorobenzoate | HCID 15621043 | 81.8% |
Reaction Steps
To a solution of 5-amino-2-fluorobenzoic acid (89.6 g, 577 mmol) in MeOH (1000 mL) was added sulfurous dichloride (82.4 g, 692 mmol) dropwise at 0° C. Then the mixture was heated to reflux for overnight. The solvent was removed. The residue was diluted with EtOAc (1 L). Then the pH was adjusted to around 9 by progressively adding saturated NaHCO3. The organic layer was separated. The aqueous layer was extracted with EtOAc (500 L×3). The combined organic layers were washed with water and brine successively, dried over Na2SO4, filtered and concentrated under reduced pressure to give the title compound of step A (79.8 g, 81.8% yield). 1H NMR (400 MHz, CDCl3) δ ppm 7.16-7.20 (m, 1H), 6.90-6.98 (m, 1H), 6.75-6.82 (m, 1H), 3.89 (s, 3H), 3.51-3.70 (br, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08642759B2 |
|---|
| Source dataset | uspto-grants-2014_02 |
|---|
| ORD ID | ord-ec0c6808cddf4126b4202b982b4d3c33 |
|---|
| Source note | uspto-grants-2014_02 |
|---|