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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129316Generated: October 30, 2026

Water → 1-(But-3-ynyloxy-methyl)-4-n-propyl-2,6,7-trithiabicyclo[2.2.2]octane

https://huagongshe.com/reaction/129316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBut-3-ynyl chloromethyl etherHCID 14868932—
Reactant4-n-Propyl-2,6,7-trithiabicyclo[2.2.2]octaneHCID 19373409—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-(But-3-ynyloxy-methyl)-4-n-propyl-2,6,7-trithiabicyclo[2.2.2]octaneHCID 19373290—

Reaction Steps

n-Butyllithium (0.3 ml,1.6M solution in hexane) was added to a solution of 4-n-propyl-2,6,7-trithiabicyclo[2.2.2]octane (0.1 g) in dry tetrahydrofuran (5 ml) at -70°, under nitrogen. The solution was stirred for 30 minutes and but-3-ynyl chloromethyl ether (0.058 g) in dry tetrahydrofuran (2.0 ml) was added and the reaction mixture was allowed to warm to 20°. Water (10 ml) was added and the mixture was extracted with diethyl ether. The ethereal extracts were dried over anhydrous magnesium sulphate and the solvent was removed in vacuo. The residue was purified by chromatography on alumina, eluting with 1:10 dichloromethane:hexane saturated with ammonia. 1-(But-3-ynyloxy-methyl)-4-n-propyl-2,6,7-trithiabicyclo[2.2.2]octane was obtained as a waxy solid (0.032 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466710
Source datasetuspto-grants-1995_11
ORD IDord-b3d62538c57a4688adcd4737c67491fc
Source noteuspto-grants-1995_11