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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725067Generated: November 3, 2026

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

https://huagongshe.com/reaction/1725067

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488822B2
Source datasetuspto-grants-2009_02
ORD IDord-852f63391d9847db9c7aea1b7cf7fdce
Source noteuspto-grants-2009_02