HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275877Generated: October 26, 2026
Dimethylformamide → 3,4-Bis(benzyloxy)benzaldehyde
https://huagongshe.com/reaction/275877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,4-Bis(benzyloxy)benzaldehyde | HCID 79526 | 182.2% |
Reaction Steps
A mixture of 3,4-dihydroxybenzaldehyde (5.0 g), benzyl bromide (14.8 g), potassium carbonate (13 g) and N,N-dimethylformamide (120 ml) was stirred for two hours at 60° C. To the reaction mixture was added cold water (200 ml), which was subjected to extraction with ethyl acetate (150 ml). The organic layer was washed with a 5% aqueous solution of potassium hydrogencarbonate, which was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 3,4-dibenzyloxybenzaldehyde (10.5 g) as colorless crystals. m.p.: 87-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352982B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-658ad29b013a48979177d9a6e4fa3286 |
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| Source note | uspto-grants-2002_03 |
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