Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090994Generated: November 1, 2026

Hydrochloric Acid → 2-Benzofurancarboxaldehyde, 3-methyl-

https://huagongshe.com/reaction/2090994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium SulfiteHCID 24437—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantEthyl 3-methyl-1-benzofuran-2-carboxylateHCID 1208056—
ReactantDiisobutylaluminumhydride tolueneHCID 86583787—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-Benzofurancarboxaldehyde, 3-methyl-HCID 13693848%

Reaction Steps

To a solution (40 mL) of ethyl 3-methyl-1-benzofuran-2-carboxylate (2.00 g) in tetrahydrofuran was added dropwise 1.5M diisobutylaluminum hydride toluene solution (19.6 mL) at 0° C., and the mixture was stirred for 2 hr. 1N Hydrochloric acid was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give a white solid. To a solution (40 mL) of the obtained solid in dichloromethane was added Dess-Martin periodinane (4.96 g) at 0° C., and the mixture was stirred at room temperature overnight. Saturated sodium sulfite aqueous solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9, volume ratio) to give the title object compound (753 mg, 48%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-9938c5c3c940443dba6d2ab343448f3d
Source noteuspto-grants-2013_05