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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691014Generated: October 25, 2026

Diethyl Ether → 4-(Hydroxy-(5-methyl-furan-2-yl)-methyl)benzaldehyde

https://huagongshe.com/reaction/1691014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant5-MethylfurfuralHCID 12097—
Reactant1-Bromo-4-(dimethoxymethyl)benzeneHCID 688342—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(Hydroxy-(5-methyl-furan-2-yl)-methyl)benzaldehydeHCID 5925533612.3%

Reaction Steps

To a mixture of 4-bromobenzaldehyde dimethyl acetal (2.0 mL, 12 mmol) and diethyl ether (30 mL) was added dropwise n-butyl lithium (1.6 M n-hexane solution, 9.0 mL, 14 mmol) at −78° C., which was stirred for 20 minutes at the same temperature. 5-Methylfurfural (1.3 mL, 13 mmol) was added dropwise into the reaction mixture at that temperature, and stirred for 50 minutes at 0° C. Water and ethyl acetate were added to extract the reaction mixture. The organic layer was washed with saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:2) to obtain the title compound (320 mg, 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-1a1839b0d51345f99fe5b6801f2fd62a
Source noteuspto-grants-2012_04