HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595371Generated: November 4, 2026
4-Hydroxybenzaldehyde → 4-(2-Methoxyethoxy)benzaldehyde
https://huagongshe.com/reaction/1595371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloroethyl methyl ether | HCID 12316 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Methoxyethoxy)benzaldehyde | HCID 6485560 | 47.9% |
Reaction Steps
4-Hydroxybenzaldehyde (300 g) and 2-chloroethyl methyl ether (279 g) were dissolved in DMF (3 L) and potassium carbonate (408 g) was added. The mixture was stirred with heating at 60° C. for 16 hr. After the reaction, the reaction mixture was poured into water and liberated oil was extracted with ethyl acetate. The organic layer was washed with 1N aqueous sodium hydroxide solution and washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate. After drying, the residue was concentrated under reduced pressure to give 4-(2-methoxyethoxy)benzaldehyde as an oil (212 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06288061B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-d6a7c5e238a047bc968413ed9a66a171 |
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| Source note | uspto-grants-2001_09 |
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