HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597874Generated: October 30, 2026
Salicylaldehyde → 2-(2-methoxyethoxy)benzaldehyde
https://huagongshe.com/reaction/1597874
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | 2-Chloroethyl methyl ether | HCID 12316 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-methoxyethoxy)benzaldehyde | HCID 11263850 | 16.6% |
Reaction Steps
To a solution of 2-hydroxybenzaldehyde (6.11 g, 0.05 mol) in DMF (50 ml) under argon in an ice bath was added NaH (2.0 g, 0.05 mol, 60% dispersion in mineral oil), followed 1 hour later by 2-chloroethylmethyl ether (4.73 g, 0.05 mol). The reaction mixture was allowed to stand for about 2 days, then was heated at 70° C. for 7 hours. The reaction mixture was stripped to dryness, the residue was partitioned between water and CHCl3, the layers were separated and the aqueous layer was extracted with CHCl3 (2×75 ml). The product appeared to be in both layers, thus they were concentrated in vacuo and the residue was purified by column chromatography on silica gel eluting with ether to afford 1.5 g of 2-[2-(methoxy)ethoxy]benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05736548 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-972883397d53416885c77496f072aad7 |
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| Source note | uspto-grants-1998_04 |
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