HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furan, 2,2'-[oxybis(methylene)]bis- → 2-{[(Furan-2-yl)methoxy]methyl}-5-methylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furan, 2,2'-[oxybis(methylene)]bis- | HCID 263034 | — |
| Reactant | 2-(Bromomethyl)-5-methylfuran | HCID 12245926 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-{[(Furan-2-yl)methoxy]methyl}-5-methylfuran | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04303689 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-7c3afd573aac40b09f8788023e17452e |
| Source note | uspto-grants-1981_12 |