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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052578Generated: November 1, 2026

Propargyl alcohol → Tetrahydro-2-(2-propynyloxy)-2H-pyran

https://huagongshe.com/reaction/2052578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantSodium CarbonateHCID 10340—
Catalystp-Toluenesulfonic acidHCID 6101—
ProductTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 9860995%

Reaction Steps

Propargyl alcohol (13.20 g) and dihydropyran (19.81 g) are placed into a 50-ml container, and 0.2 g of anhydrous p-toluenesulfonic acid is added. The mixture is cooled in an ice bath, then stirred at room temperature for 30 minutes and neutralized with anhydrous sodium carbonate. The resulting solids are separated off. Distillation of the remaining liquid in a vacuum gives 31.3 g of propargyl tetrahydropyranyl ether (yield: 95%), b.p. 75° to 80° C./37 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04186141
Source datasetuspto-grants-1980_01
ORD IDord-241dbcadfc6646149c7014b6a3e1a3fb
Source noteuspto-grants-1980_01