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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579657Generated: November 2, 2026

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

https://huagongshe.com/reaction/1579657

Reaction equation

Participants

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

Reaction Steps

1 d. 5-Methyl-furfuryl furfuryl ether was prepared by the procedure described by J. E. Zanetti in J. Am. Chem. Soc. 49, 1066 (1927) for the difurfuryl ether, starting with 5-methylfurfuryl 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 numberUS03931246
Source datasetuspto-grants-1976_01
ORD IDord-37b52a200b874f52ae6f33cdf97532e6
Source noteuspto-grants-1976_01