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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659366Generated: October 29, 2026

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

https://huagongshe.com/reaction/1659366

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

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 numberUS04303689
Source datasetuspto-grants-1981_12
ORD IDord-7c3afd573aac40b09f8788023e17452e
Source noteuspto-grants-1981_12