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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452466Generated: October 31, 2026

Potassium Carbonate → Methyl 2-fluoro-6-hydroxy-4-(methylsulfonyl)benzoate

https://huagongshe.com/reaction/452466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantL-ProlineHCID 145742—
ReactantSodium methanesulfinateHCID 2733271—
ReactantMethyl 4-bromo-2-fluoro-6-hydroxybenzoateHCID 66886502—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 2-fluoro-6-hydroxy-4-(methylsulfonyl)benzoateHCID 6688748410.1%

Reaction Conditions

Temperature95 °C

Reaction Steps

Methyl 4-bromo-2-fluoro-6-hydroxybenzoate (1.7 g, 5.6 mmol), sodium methanesulfinate (95%) (0.91 g, 8.5 mmol), CuI (0.64 g, 3.4 mmol), L-proline (0.78 g, 6.8 mmol) and K2CO3 (0.47 g, 3.4 mmol) was dissolved in DMSO (dry) (10 ml). Nitrogen was bubbled through the solution for 15 min. The mixture was stirred and heated at 95° C. for 6 h under nitrogen. After cooling to RT, the mixture was filtered on a plug of silica and eluted with ETOAc. The filtrate was washed with 1M citric acid. The waterlayer was extracted once with EtOAc. The combined organic phases were washed with brine, dried (Na2SO4), filtered and concentrated. Purification on flash column chromatography (isooctane/EtOAc) gave the crude title compound (0.14 g). MS m/z (rel. intensity, 70 eV) 248 (M+, 36), 216 (bp), 173 (19), 125 (20), 81 (24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492372B2
Source datasetuspto-grants-2013_07
ORD IDord-72180e4894a74bbeb598f96ca12253a8
Source noteuspto-grants-2013_07