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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271247Generated: November 2, 2026

1,4-Butanediol → 4-(Tetrahydro-2H-pyran-2-yloxy)-1-butanol

https://huagongshe.com/reaction/1271247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-ButanediolHCID 8064—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(Tetrahydro-2H-pyran-2-yloxy)-1-butanolHCID 559113—

Reaction Steps

To a solution of 100.0 g of 1,4-butanediol and 20 ml of 3,4-dihydro-2H-pyrane in 80 ml of dichloromethane and 140 ml of tetrahydrofuran, 1.8 g of pyridinium p-toluenesulfonate was added. After stirring at room temperature for 18 hours, the solvent was evaporated under reduced pressure. The residue was extracted three times with diethyl ether after adding saturated brine. After the extract was washed with a small amount of water and dried over anhydrous magnesium sulfate, the solvent was evaporated to obtain 35.98 g of the desired crude product as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205302B2
Source datasetuspto-grants-2007_04
ORD IDord-44b9cf5e8c6e40888a85d7303687e717
Source noteuspto-grants-2007_04