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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569840Generated: October 25, 2026

Cyanic acid → Tetrahydropyranyl ether

https://huagongshe.com/reaction/569840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanic acidHCID 540—
ReactantDiethyl EtherHCID 3283—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-dihydro-2H-pyranHCID 8080—
SolventDichloromethaneHCID 6344—
ProductTetrahydropyranyl etherHCID 263182—

Reaction Steps

A solution of 1.23 g of Part A(6) cyano-alcohol (7.36 mmole) in 20 ml of dry methylene chloride was treated with 800 ml of dihydropyran (8.89 mmole) and catalytic amount of p-toluene sulfonic acid at 0°-5° C. After 4 hours, the reaction mixture was diluted with ether and washed with aqueous sodium bicarbonate solution. The aqueous layer was reextracted twice with ether. The combined organic extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The crude residue was chromatographed on a silica gel column and eluted with 20-25% ethyl acetate in hexane to obtain 1.61 g of title tetrahydropyranyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734426
Source datasetuspto-grants-1988_03
ORD IDord-78b12154850d4e2eb26cf9612f3e568f
Source noteuspto-grants-1988_03