Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369931Generated: October 31, 2026

Methanol → Methyl 2-fluoro-3-methylbenzoate

https://huagongshe.com/reaction/2369931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Fluoro-3-methylbenzoic acidHCID 2737379—
ProductMethyl 2-fluoro-3-methylbenzoateHCID 22049929100%

Reaction Steps

To a solution of 2-fluoro-3-methylbenzoic acid (12.4 g, 80.2 mmol) in methanol (100 mL) at 0° C. was added thionyl chloride (14 g, 120.3 mmol) dropwise. The reaction mixture was stirred at reflux until complete by TLC (1-2 h). After cooling to room temperature, the mixture was partitioned between sat. NaHCO3 and ethyl acetate. The combined organic layers were dried (Na2SO4), filtered and concentrated to give methyl 2-fluoro-3-methylbenzoate as a yellow oil (13.8 g, 100%): 1H NMR (300 MHz, CDCl3) δ 7.74 (t, J=8.1 Hz, 1H), 7.37 (t, J=7.8 Hz, 1H), 7.08 (t, J=7.5 Hz, 1H), 3.90 (s, 3H), 2.31 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710046B2
Source datasetuspto-grants-2014_04
ORD IDord-fcd6e899b9294871866026af80c1ea6d
Source noteuspto-grants-2014_04