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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068Generated: October 23, 2026

2-Butyne-1,4-diol → 4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-ol

https://huagongshe.com/en/reaction/2068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butyne-1,4-diolHCID 8066—
Reactant3,4-dihydro-2H-pyranHCID 8080—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventDiethyl EtherHCID 3283—
Product4-(Tetrahydro-pyran-2-yloxy)-but-2-yn-1-olHCID 1112331568.8%

Reaction Steps

To a mixture of 5.0 g of 2-butyne-l,4-diol and 10 milligrams of p-toluenesulfonic acid and 150 ml of dry ether there was added dropwise with stirring at room temperature 4.9 g of 3,4-dihydro-2H-pyran. After stirring overnight at ambient temperature the ether was evaporated and the residue was poured into 200 ml of water. The aqueous solution was extracted with hexane (2×100 ml) and then re-extracted with ether (3×100 ml). The combined ether extracts were washed with 100 ml of brine, dried over magnesium sulfate and evaporated to yield 6.8 g of 4-tetrahydropyranoxy-2-butyn-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728694
Source datasetuspto-grants-1998_03
ORD IDord-b5f509f406ce44cc9d59d96a369153b8
Source noteuspto-grants-1998_03