HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → Methyl 3-fluoro-2-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 3-Fluoro-2-methylbenzoic acid | HCID 246682 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-fluoro-2-methylbenzoate | HCID 21752566 | 87% |
Reaction Steps
A solution of 3-fluoro-2-methyl-benzoic acid (Aldrich, 10.2 g, 66.17 mmol) in methanol (135 mL) at room temperature was treated with boron trifluoride etherate (15 mL) and was allowed to stir at room temperature. The reaction mixture was then concentrated in vacuo to remove the methanol and then diethyl ether (−300 mL) was added. The solution was transferred to a separatory funnel and washed with water (200 mL) and a 5% aqueous sodium bicarbonate solution to pH>7.5. The organic layer was then dried over magnesium sulfate and concentrated in vacuo to afford 3-fluoro-2-methyl-benzoic acid methyl ester (9.74 g, 87%) as a light orange colored oil which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697705B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-401291ac9df1416e84974949fea9cbcf |
| Source note | uspto-grants-2014_04 |