HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15250Generated: November 1, 2026
Dimethylformamide → 3,5-Bis(methoxymethyl)benzaldehyde
https://huagongshe.com/reaction/15250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-bromo-3,5-bis(methoxymethyl)Benzene | HCID 15134211 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Bis(methoxymethyl)benzaldehyde | HCID 15134212 | 79% |
Reaction Steps
Grignard solution was prepared from 13.4 g (54.7 mmol) of 3,5-bis(methoxymethyl)bromobenzene, 3.25 g (134 mmol) of magnesium, and 60 ml of tetrahydrofuran (hereinafter abbreviated as “THF”) in a reaction vessel of 200 ml. Subsequently, 30 ml (387 mmol) of dimethylformamide (DMF) was added dropwise into this solution at 0° C. and further agitated at room temperature for 3 hours after completion of the addition. Solvent was removed from the obtained reaction liquid by reduced pressure and 2N hydrochloric acid was added. The obtained reaction mixture was extracted 3 times with 50 ml of diethyl ether and the organic layer was collected and dried with anhydrous magnesium sulfate after rinsing with water. Residues obtained by the removal of solvent were purified by silica gel column chromatography to obtain 8.36 g (43.0 mmol) of the target 3,5-bis(methoxymethyl)benzaldehyde as a viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732549B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-dff83f2dd8594112a6b0b3b03b38150e |
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| Source note | uspto-grants-2010_06 |
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