HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248559Generated: October 30, 2026
Water → 2-Methoxymethyloxy-3,4,5,6-tetramethoxybenzaldehyde
https://huagongshe.com/reaction/248559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Methoxymethyloxy-2,3,4,5-tetramethoxybenzene | HCID 13495532 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Methoxymethyloxy-3,4,5,6-tetramethoxybenzaldehyde | HCID 13495550 | — |
Reaction Steps
6.2 g of 1-methoxymethyloxy-2,3,4,5-tetramethoxybenzene prepared in Referential Example 13 was dissolved in 50 ml of anhydrous ether, and 18 ml of n-butyllithium (1.6 M n-hexane solution) was dropwise added thereto at -20° C. while stirring. After the mixture was stirred at 0° C. for 30 min, the temperature was returned to -20° C. and 3.5 ml of DMF was dropwise added thereto. After 100 ml of water was added thereto, the mixture was extracted with ethyl acetate, and the organic phase was washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (eluent; n-hexane : ethyl acetate=7 : 3) to prepare 5.6 g of the product compound as a light yellow oleaginous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05210239 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-d6ad9c572247489999f2e294f7a20a44 |
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| Source note | uspto-grants-1993_05 |
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