HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381731Generated: October 26, 2026
Water → 3,4-Bis(methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/381731
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Product | 3,4-Bis(methoxymethoxy)benzaldehyde | HCID 11746314 | — |
Reaction Steps
Chloromethyl methyl ether (1.2 ml, 15.8 mmol) was added dropwise to a stirred solution containing 3,4-dihydroxybenzaldehyde (1 g, 7.25 mmol) and triethylamine (2 ml) in dimethylformamide (100 ml). After stirring at room temperature for 2 days, water (100 ml) was added to destroy any excess chloromethyl methyl ether. The reaction mixture was extracted with ethyl acetate (2×250 ml). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo to give a brown syrup. The crude mixture was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexanes (1:4) to give first 3,4-bismethoxymethoxybenzaldehyde (0.4 g) as a light yellow syrup, and then the monomethoxymethylated derivatives of 3,4-dihydroxybenzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06307070B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-15498dc6aac749799f41f9c64f889f08 |
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| Source note | uspto-grants-2001_10 |
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