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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264519Generated: November 4, 2026

p-Toluenesulfonic acid → Methyl 3-bromo-2-fluorobenzoate

https://huagongshe.com/reaction/1264519

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTrimethyl orthoformateHCID 9005—
Reactant3-Bromo-2-fluorobenzoic acidHCID 2736313—
SolventMethanolHCID 887—
ProductMethyl 3-bromo-2-fluorobenzoateHCID 2158450584%

Reaction Steps

A solution of 3-bromo-2-fluorobenzoic acid. (0.219 g, 1 mmol) in dry methanol (5 ml) under nitrogen was treated with trimethylorthoformate (0.22 ml, 2 mmol) and p-toluenesulfonic acid (catalytic amount), and then heated under reflux. After 16 h, the mixture was evaporated and the residue partitioned between water and Et2O. The organic layer was washed with sat. sodium hydrogen carbonate solution, water, brine, dried (MgSO4) and evaporated to give methyl 3-bromo-2-fluorobenzoate (0.195 g, 0.84 mmol, 84%): 1H NMR (CDCl3) δ 7.90-7.85 (m, 1H), 7.71-7.65 (m, 1H), 7.10 (dt, 1H, J=8.0, 1.0 Hz) and 3.94 (s, 3H): MS (EI) 232 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544970B2
Source datasetuspto-grants-2003_04
ORD IDord-0ec6fe9450f64b1ab7bfbbd45dd56b74
Source noteuspto-grants-2003_04