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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990663Generated: October 30, 2026

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

https://huagongshe.com/reaction/990663

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 numberUS06462032B1
Source datasetuspto-grants-2002_10
ORD IDord-5fb51c63036e410b835fd779d4c43d2b
Source noteuspto-grants-2002_10