Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345364Generated: October 30, 2026

Tetrabutylammonium Fluoride → 2,6,7-Trioxabicyclo(2.2.2)octane, 4-ethyl-1-(4-ethynylphenyl)-

https://huagongshe.com/reaction/345364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 15021947HCID 15021947—
SolventTetrahydrofuranHCID 8028—
Product2,6,7-Trioxabicyclo(2.2.2)octane, 4-ethyl-1-(4-ethynylphenyl)-HCID 306569198.3%

Reaction Steps

Tetrabutyl ammonium fluoride solution (3.3 ml, 1M in tetrahydroforan) was added to a stirred solution of 4-ethyl-1-[4-(2-trimethylsilylethynyl)phenyl]-2,6,7-trioxabicyclo[2,2,2]octane (0.87 gms) in tetrahydrofuran (15 ml). The mixture was stirred for 30 minutes at room temperature when the solvent was removed under vacuum. The residue was taken up in ether and washed with water and brine. The ethereal solution was dried over anhydrous magnesium sulphate and evaporated in vacuo. Recrystallisation from hexane gave 4-ethyl-1-(4-ethynylphenyl)-2,6,7-trioxabicyclo[2,2,2]octane as an off-white solid (0.66 gms).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057508
Source datasetuspto-grants-1991_10
ORD IDord-9699f4cef7984ea5ab061c8806358406
Source noteuspto-grants-1991_10