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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-(p-Methoxybenzyl)-3-methyl-4-hydroxy-5-propylbenzofuran | HCID 14570889 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-Formyl-4-methoxybenzyl)-3-methyl-4-hydroxy-5-propyl-benzofuran | HCID 15029652 | 37% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04863958 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-1fe1bb83fd534b55a29d2378f5d57785 |
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| Source note | uspto-grants-1989_09 |
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