HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505661Generated: October 31, 2026
Methanol → 2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/505661
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromo-1-(benzyloxymethyl)-3,5-bis(methoxymethoxy)benzene | HCID 23147594 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(Benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde | HCID 21669817 | 72% |
Reaction Steps
The above-obtained 2-bromo-1-(benzyloxymethyl)-3,5-bis(methoxymethoxy)benzene (1.6 g, 4.3 mmol) was dissolved in diethylether (25 mL) and cooled to −78° C. The obtained solution was added with 1.52 mol/L n-butyllithium-hexane solution (4.0 mL, 6.1 mmol) and stirred at −78° C. for 1 hour. Then, N,N-dimethylformamide (1.0 mL, 13 mmol) was added thereto and stirred at a room temperature for 3 hours. The reaction mixture was added with water and methanol, and then extracted with chloroform 3 times. The organic layers were combined, washed with saturated brine, and then dried over anhydrous sodium sulfate. Then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1 to 5/1 to 3/1) to obtain 2-(benzyloxymethyl)-4,6-bis(methoxymethoxy)benzaldehyde (0.99 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781485B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-4f6fedc485ba409ca1005d609e123232 |
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| Source note | uspto-grants-2010_08 |
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