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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607242Generated: November 1, 2026

Water → 2-(3-Formyl-4-methoxybenzyl)-3-methyl-4-hydroxy-5-propyl-benzofuran

https://huagongshe.com/reaction/1607242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethane, dichloromethoxy-HCID 21004—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-(p-Methoxybenzyl)-3-methyl-4-hydroxy-5-propylbenzofuranHCID 14570889—
SolventDichloromethaneHCID 6344—
Product2-(3-Formyl-4-methoxybenzyl)-3-methyl-4-hydroxy-5-propyl-benzofuranHCID 1502965237%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of aluminium chloride (214 mg; 1.6mmole) in dichloromethane (5 mL) cooled at 0° C. was added 2-(p-methoxy benzyl)-3-methyl-4-hydroxy-5-propyl benzofuran (100 mg; 0.32mmoles). A red solution resulted. To this solution was added dropwise dichloromethylmethylether (87 (1; 0.96 mmole). There was a vigorous reaction and a color change from red to green was observed. Ice and water was then added and the mixture was extracted with ethylacetate. The organic phase was dried (Na2SO4), and concentrated in vacuo and the residue was chromatographed on silica gel. Elution with 10% ethylacetate in hexane yielded 40 mg (37%) of 2-(3 formyl-4-methoxybenzyl)-3-methyl-4-hydroxy-5-propyl-benzofuran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863958
Source datasetuspto-grants-1989_09
ORD IDord-1fe1bb83fd534b55a29d2378f5d57785
Source noteuspto-grants-1989_09