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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517129Generated: November 4, 2026

Furan → HCID 21224573, compound

https://huagongshe.com/reaction/1517129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
Reactant5-(Ethoxymethyl)furan-2-carbaldehydeHCID 12648080—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
ProductHCID 21224573HCID 2122457380%

Reaction Steps

In a 7.5 ml batch reactor, 0.06 mmol 5-(ethoxymethyl)furfural (EMF) in 1 mL ethanol and 5 bars of hydrogen was reacted with 3 mol % of a Pt/C catalyst for 4 days at room temperature. The starting material was completely converted in 100% selectivity to 5-(ethoxymethyl)-2-hydroxymethyl)furan. Subsequently, the mixture was heated to 75° C. for 1 day without hydrogen. The 5-(ethoxymethyl)-2-hydroxymethyl)furan was fully converted and 2,5-bis(ethoxymethyl)furan was obtained in 80% yield. 20% Side products are ring opened levulinate derivatives. The experiment was successfully repeated on a 20 gram scale.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08231693B2
Source datasetuspto-grants-2012_07
ORD IDord-afb06bf215504869b70f16bbcac0c03b
Source noteuspto-grants-2012_07