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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936951Generated: October 31, 2026

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

https://huagongshe.com/reaction/1936951

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) δ7.90-7.85 (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 numberUS06391907B1
Source datasetuspto-grants-2002_05
ORD IDord-fa9d371a427245d1970472cb207e4af9
Source noteuspto-grants-2002_05