Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579232Generated: November 1, 2026

Furan, 2,2'-[oxybis(methylene)]bis- → 2-{[(Furan-2-yl)methoxy]methyl}-5-methylfuran

https://huagongshe.com/reaction/1579232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuran, 2,2'-[oxybis(methylene)]bis-HCID 263034—
Reactant2-(Bromomethyl)furanHCID 4603765—
Reactant2-(Bromomethyl)-5-methylfuranHCID 12245926—
SolventDiethyl EtherHCID 3283—
Product2-{[(Furan-2-yl)methoxy]methyl}-5-methylfuranHCID 20560356—

Reaction Steps

d. 5-Methyl-furfuryl furfuryl ether is prepared by the procedure described by J. E. Zanetti in J.Am.Chem.Soc. 49, 1066 (1927) for the difurfuryl ether, starting with 5-methyl-furfuryl bromide (Compt, Rend. 222, 1441 (1946) instead of furfuryl bromide of Zanetti. The product was isolated by ether extraction of the crude mixture after having diluted with water. For purification the ether extract was distilled twice -- b.p. 68°-70°C. at 0.01 mm./Hg vacuum. The product was a viscous colourless liquid, darkening rapidly on contact with air.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931166
Source datasetuspto-grants-1976_01
ORD IDord-d86a43e285094528879b7fe296798f3b
Source noteuspto-grants-1976_01