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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634984Generated: November 1, 2026

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

https://huagongshe.com/reaction/1634984

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), 3.94 (s, 3H): MS (EI) 232 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509334B1
Source datasetuspto-grants-2003_01
ORD IDord-c8ea8863b6e24c078a72506f62f48a12
Source noteuspto-grants-2003_01