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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55548Generated: October 25, 2026

2-Fluoroethanol → 3-(2-Fluoroethoxy)-pyrid-2-ylsulfonamide

https://huagongshe.com/reaction/55548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroethanolHCID 9737—
ReactantSodium hydrideHCID 24758—
Reactant3-Fluoropyridine-2-sulfonamideHCID 19957930—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Fluoroethoxy)-pyrid-2-ylsulfonamideHCID 19957936—

Reaction Steps

5.76 ml of 2-fluoroethanol are added dropwise, with cooling, to a suspension of 6.54 g of sodium hydride (55.6% NaH in oil) in 120 ml of tetrahydrofuran so that the temperature does not exceed 20° C. When the dropwise addition is complete, the reaction mixture is stirred at room temperature for 15 minutes and then a further solution of 10.56 g of 3-fluoro-pyrid-2-ylsulfonamide in 60 ml of tetrahydrofuran is added dropwise over a period of 10 minutes. The reaction solution is then stirred for 10 minutes at room temperature and for 2 hours at reflux before it is cooled and concentrated. For purification, the oil remaining is chromatographed on a silica gel column using ethyl acetate/hexane 4/1. Evaporation of the eluant yields a light-coloured oil which crystallises spontaneously, yielding 5.88 g of title product which melts at 122°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05625071
Source datasetuspto-grants-1997_04
ORD IDord-a73cb883fae1487ca599634bf5ed7e4b
Source noteuspto-grants-1997_04