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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253391Generated: October 31, 2026

Water → 1,4-Diethynyl-2,5-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzene

https://huagongshe.com/reaction/1253391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67251592HCID 67251592—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1,4-Diethynyl-2,5-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}benzeneHCID 25127627—

Reaction Steps

1,4-bis[(trimethylsilyl)ethynyl]-2,5-bis[2-[2-(2-ethoxyethoxy)ethoxy]ethoxy]benzene (0.595 g, 1 mmol) was dissolved in 20 mL of THF and 10 mL of methanol. To the solution, 8 mL of 1M NaOH(aq) was added and refluxed for 2 hours. Water was added to the mixture and extracted with ether. The organic layer was washed with water several times, and then dried with Na2SO4. Solvent was removed by rotary evaporation to give 1,4-diethynyl-2,5-bis[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]benzene (3), shown in FIG. 2, as a reddish solid. 1H NMR (300 MHz, CDCl3): d 3.32 (s, 2H), 3.36 (s, 6H), 3.53 (m, 4H), 3.65 (m, 8H), 3.75 (m, 4H), 3.85 (m, 4H), 4.13 (m, 4H), 6.98 (s, 2H). 13C NMR (75 MHz, CDCl3): d 59.46, 69.96, 70.03, 71.00, 71.15, 71.50, 72.39, 80.00, 83.22, 114.02, 118.75, 154.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455265B2
Source datasetuspto-grants-2013_06
ORD IDord-2871bf8b840343a4aafa6e26c4a818be
Source noteuspto-grants-2013_06