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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375290Generated: October 31, 2026

Potassium Carbonate → HCID 22273513, compound

https://huagongshe.com/reaction/2375290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromothiophenolHCID 66049—
Reactant3-Methoxypropyl methanesulfonateHCID 11693963—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 22273513HCID 2227351362%

Reaction Conditions

Temperature40 °C

Reaction Steps

Potassium carbonate (2.8 g, 20 mmol) was added to a solution of 3-methoxypropan-1-yl methansulphonate (Method 68; 3.25 g, 19.3 mmol) and 4-bromothiophenol (3.48 g, 18.4 mmol) in DMF (30 ml) and the mixture heated at 40° C. for 4 hours. The mixture was allowed to cool to ambient temperature, poured into water (100 ml) and extracted with EtOAc (2×50 ml). The extracts were combined, washed with saturated aqueous sodium hydrogen carbonate solution (50 ml) and brine (2×50 ml), dried (Chemelut column CE1010) and the volatiles removed by evaporation. The residue was dissolved in MeOH (150 ml) and water (30 ml) and oxone (13.4 g, 21.6 mmol) was added in portions. The mixture was stirred at ambient temperature for 18 hours. The MeOH was evaporated, water (50 ml) added and the solution extracted with DCM (3×50 ml). The extracts were combined, washed with brine (50 ml), dried (Chemelut column CE1010), and evaporated. The residue was purified by flash chromatography on silica gel eluting with iso-hexane: EtOAc (100:0 increasing in polarity to 90:10) to give the title compound (3.32 g, 62%) as a colourless oil. NMR 1.95 (m, 2H), 3.19 (m, 2H), 3.26 (s, 3H), 3.41 (t, 2H), 7.70 (d, 2H), 7.78 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465728B2
Source datasetuspto-grants-2008_12
ORD IDord-0c2d5f05652446ce803a54d6d5ede578
Source noteuspto-grants-2008_12