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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195916Generated: November 1, 2026

Acetaldehyde → 3-(Furan-3-yl)prop-2-enal

https://huagongshe.com/reaction/1195916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant3-FuraldehydeHCID 10351—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3-(Furan-3-yl)prop-2-enalHCID 5369276841%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2N NaOH (115 mL) was added 3-furaldehyde (4.5 mL, 52.0 mmol) dropwise. The solution was stirred until homogeneous (approximately five minutes) and then cooled to 0° C. and acetaldehyde (1.65 mL, 57.2 mmol) in 5 mL water was added. The reaction was stirred at 0° C. for 30 min and was then diluted with ether. The mixture was separated and the aqueous layer was extracted with ether (3×50 mL). The combined organic extract was washed with brine, dried over MgSO4, filtered and evaporated to yield 4.56 g of crude product. Chromatography (silica gel ,30% ether/hexanes) yielded 2.6 g (41%) of 3-(furan-3-yl)propenal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112848
Source datasetuspto-grants-1992_05
ORD IDord-2405e1118cce40eeb5a60aa6dd0f0044
Source noteuspto-grants-1992_05