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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261497Generated: November 1, 2026

Boron trifluoride etherate → Methyl 3-fluoro-2-methylbenzoate

https://huagongshe.com/reaction/1261497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant3-Fluoro-2-methylbenzoic acidHCID 246682—
SolventMethanolHCID 887—
ProductMethyl 3-fluoro-2-methylbenzoateHCID 2175256687%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470866B2
Source datasetuspto-grants-2013_06
ORD IDord-b1b703bc45074664a0a5817441bdb59e
Source noteuspto-grants-2013_06