HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413789Generated: October 25, 2026
Water → 2-(Benzyloxy)-3-methoxybenzaldehyde
https://huagongshe.com/reaction/413789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | o-Vanillin | HCID 8991 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Benzyloxy)-3-methoxybenzaldehyde | HCID 1268087 | 81% |
Reaction Steps
Benzyl bromide (8.6 ml) was added to a stirred solution of 3-methoxysalicylaldehyde (10 g), potassium carbonate (14.76 g) and potassium iodide (0.12 g) in DMF (120 ml) under an atmosphere of argon. The reaction was heated at 70° C. for 16 hours. Water (200 ml) was added causing the precipitation of a brown oil which crystallised on cooling. The solid was filtered, washed with water, dissolved in dichloromethane and dried (MgSO4). The solvent was removed in vacuo to give an oil which crystallised on trituration with iso-hexane to give the product as an off white solid (12.85 g, 81%); NMR d (CD3SOCD3) 3.91 (s, 3H), 5.15 (s, 2H), 7.14-7.22 (m, 2H), 7.29-7.42 (m, 6H), 10.10 (t, 1H); M/z (+) 243 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06569888B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-85cf6ef0ec784178b2581fde72b3ab84 |
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| Source note | uspto-grants-2003_05 |
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