Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046445Generated: October 30, 2026

Potassium Carbonate → 3-(2,2-Dimethyl-but-3-ynyloxy)-tetrahydro-furan

https://huagongshe.com/reaction/1046445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,2-Dimethyl-3-(tetrahydro-furan-3-yloxy)-propionaldehydeHCID 58114068—
Reactant(1E)-1-diazo-1-dimethoxyphosphorylpropan-2-oneHCID 136023029—
SolventMethanolHCID 887—
Product3-(2,2-Dimethyl-but-3-ynyloxy)-tetrahydro-furanHCID 5811389469.3%

Reaction Steps

(1-Diazo-2-oxo-propyl)-phosphonic acid dimethyl ester (418 mg, 2.17 mmol) was added to a stirred suspension of 2,2-dimethyl-3-(tetrahydro-furan-3-yloxy)-propionaldehyde (250 mg, 1.45 mmol) and K2CO3 (601 mg, 4.35 mmol) in methanol (17.0 mL) at room temperature. After overnight stirring the bulk of the methanol was removed by rotary evaporation and the reaction mixture partitioned between ethyl ether and NaHCO3. The organic layer was separated, washed with brine, dried over Na2SO4 and concentrated to provide a crude liquid. Purification by flash column chromatography on silica gel using 30% ethyl acetate in hexanes followed by bulb to bulb distillation under reduced pressure provided 3-(2,2-dimethyl-but-3-ynyloxy)-tetrahydro-furan (169 mg, 69%) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569302B2
Source datasetuspto-grants-2013_10
ORD IDord-98354c45ae644b1c8ee0ef5e70b1982b
Source noteuspto-grants-2013_10