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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390235Generated: November 1, 2026

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

https://huagongshe.com/reaction/1390235

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

d. 5-Methyl-furfuryl furfuryl ether was prepared by the procedure described in 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 numberUS04138410
Source datasetuspto-grants-1979_02
ORD IDord-e9150b1588064ec8bbbf5b11ffe02f20
Source noteuspto-grants-1979_02