HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488116Generated: October 29, 2026
Water → 5-Ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehyde
https://huagongshe.com/reaction/488116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Ethyl-4-hydroxy-3-methoxy-1-naphthalenecarbaldehyde | HCID 10263239 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehyde | HCID 9970569 | — |
Reaction Steps
324 g of 5-ethyl-4-hydroxy-3-methoxy-1-naphthalenecarbaldehyde was dissolved in 1 liter of N,N-dimethylformaldehyde, to which 68 g of 60% sodium hydride was gently added under ice-cooling conditions. After agitation for 10 minutes, 128 ml of chloromethyl methyl ether was gradually added so that the reaction temperature did not exceed 15° C. After agitation at room temperature for 20 minutes, the reaction solution was poured into iced water and extracted with ethyl acetate. The resultant organic phase was washed with a saturated saline solution and dried with anhydrous magnesium sulfate. The solvent was distilled off and the resultant residue was purified by silica gel column chromatography (5% ethyl acetate/hexane) to obtain 288 g of the captioned compound as a brown oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298649 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-1425fbee7f1f455f91ce2dd4b60c680e |
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| Source note | uspto-grants-1994_03 |
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