HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217427Generated: October 30, 2026
Ethyl Acetate → 7-(methoxymethoxy)-2,2-dimethyl-2H-chromene-3-carbaldehyde
https://huagongshe.com/reaction/217427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Methyl-2-butanone | HCID 11251 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-4-(methoxymethoxy)benzaldehyde | HCID 2755073 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 7-(methoxymethoxy)-2,2-dimethyl-2H-chromene-3-carbaldehyde | HCID 58438670 | — |
Reaction Steps
K2CO3 (835 mg) was suspended in dioxane (40 mL), and 2-hydroxy-4-(methoxymethoxy)benzaldehyde (1 g) and 3-methyl 2-butanal (0.787 mL) were added thereto, followed by stirring at 110° C. overnight. EtOAc was added thereto, the insoluble materials were removed by filtration through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (automatic purification device, hexane:EtOAc=95:5 to 70:30) to obtain 7-(methoxymethoxy)-2,2-dimethyl-2H-chromene-3-carbaldehyde (320 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193378B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-99671a6d4e1c40538f60cbc2acc091cd |
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| Source note | uspto-grants-2012_06 |
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