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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273340Generated: October 30, 2026

Hydrochloric Acid → 6-Methoxy-2-methylbenzofuran-3-carbaldehyde

https://huagongshe.com/reaction/273340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-[1,3]Dioxolan-2-yl-6-methoxy-2-methyl-benzofuranHCID 69194253—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-2-methylbenzofuran-3-carbaldehydeHCID 8660618881%

Reaction Steps

2N HCl (5 mL) was added to 3-[1,3]dioxolan-2-yl-6-methoxy-2-methyl-benzofuran in THF (5 mL) at 0° C. After stirring for 1 h at room temperature, the solvent was removed under reduced pressure. The residue was dissolved in EtOAc and washed with saturated NaHCO3. The aqueous layer was extracted with EtOAc (3×20 mL). The organic layers were combined and dried over anhydrous MgSO4. After the solvent was removed, the residue was purified on a silica gel column eluting with EtOAc/hexane (1:9) to give 6-methoxy-2-methylbenzofuran-3-carbaldehyde (0.090 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456289B2
Source datasetuspto-grants-2008_11
ORD IDord-ffd0ed48999a4c6386934c56f12c0b3c
Source noteuspto-grants-2008_11