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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424690Generated: October 29, 2026

Carbon Dioxide → 2-Fluoro-3-methoxybenzoic acid

https://huagongshe.com/reaction/424690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant2-FluoroanisoleHCID 67576—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product2-Fluoro-3-methoxybenzoic acidHCID 3390679—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Pentamethylenediethylenetetramine (31.2 ml) was added to a solution of 2-fluoroanisole (15.0 g) in THF (450 ml). The reaction mixture was cooled to −78° C. and n-butyllithium (59.6 ml, 2.5M solution in hexanes) was added dropwise. Stirring was maintained for 2 h before the solution was added in a dropwise fashion to a flask containing solid carbon dioxide pellets. Upon complete addition (30 min) the mixture was allowed to warm to room temperature before removal of the volatiles in vacuo. The residue was dissolved in 10% sodium hydroxide solution (300 ml) and extracted with Et2O (3×). The aqueous was acidified to pH 1 with concentrated hydrochloric acid before extracting with DCM. The organics were washed with H2O, dried (MgSO4) and concentrated in vacuo to afford the subtitle compound as a yellow solid. Yield: 7.1 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106063B2
Source datasetuspto-grants-2012_01
ORD IDord-7bf291c6512e483fac443a9db0564a00
Source noteuspto-grants-2012_01