HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 3-bromo-2,4,5-trifluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Bromo-2,4,5-trifluorobenzoyl fluoride | HCID 14149872 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl 3-bromo-2,4,5-trifluorobenzoate | HCID 18459836 | — |
Reaction Steps
772 g of 3-bromo-2,4,5-trifluoro-benzoylfluoride are added dropwise with ice-cooling to a mixture of 1460 ml of methanol and 340 g of triethylamine. Stirring is carried out at room temperature for 1 hour. The reaction mixture is concentrated, the residue is taken up in water and methylene chloride, and the aqueous phase is again extracted by shaking with methylene chloride. After drying the organic phase over sodium sulphate, it is concentrated and the residue is distilled in vacuo. 752.4 g of methyl 3-bromo-2,4,5-trifluoro-benzoate of boiling point 122° C./20 mbar are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133260 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-9bb366711f7b4f87b41193cf93bbfc82 |
| Source note | uspto-grants-2000_10 |