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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051033Generated: October 23, 2026

5-Chloromethylfurfural → 5-Acetoxymethyl-2-furaldehyde

https://huagongshe.com/en/reaction/1051033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-ChloromethylfurfuralHCID 74191—
ReactantHCID 178476379HCID 178476379—
SolventAcetonitrileHCID 6342—
Product5-Acetoxymethyl-2-furaldehydeHCID 66349—

Reaction Steps

In a round flask, 2 mL of methyl cyanide (acetonitrile) as an organic solvent was introduced, 0.145 g (1 mmol) of 5-chloromethylfurfural (CMF, compound I) was dissolved in the organic solvent, 0.170 g (1 mmol) of 1-ethyl-3-methylimidazolium acetate was added to the solution, and then the mixed solution was reacted at normal pressure and room temperature for 5 minutes. After the reaction, the reaction product was extracted by the addition of a small amount of water (5 mL) and ethyl acetate (added twice by 20 mL) to obtain an organic layer. The obtained organic layer was concentrated under reduced pressure to obtain light yellow liquid 5-acetoxymethylfurfural (AcHMF, compound II). The yield thereof is 36%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388150B2
Source datasetuspto-grants-2016_07
ORD IDord-fa13fc02b128447c81c9ce0551e8f51c
Source noteuspto-grants-2016_07