HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725584Generated: November 4, 2026
Vanillin → 3-Methoxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde
https://huagongshe.com/reaction/1725584
Participants
| Role | Name | HCID | Charge |
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| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxy-4-[(4-methoxyphenyl)methoxy]benzaldehyde | HCID 2764492 | 84.6% |
Reaction Steps
A mixture of 4-hydroxy-3-methoxybenzaldehyde (22.6 g, 149 mmol), 4-methoxybenzyl chloride (23.3 g, 149 mmol) and potassium carbonate (30.8 g, 223 mmol) was stirred in N,N-dimethylformamide (DMF) (150 mL) at 90 C for 2 hours. The solution was filtered hot, and cooled to room temperature. The filtrate was concentrated and dissolved ethyl acetate (300 mL) and extracted with aqueous sodium bicarbonate and water. The organics were dried with magnesium sulfate, filtered and concentrated. The crude product was recrystalized with ethyl acetate and hexanes to give product as an off-white solid (34.2 g, 126 mmol). 1H NMR (300 MHz, d6-DMSO): δ 9.86 (s, 1H), 7.58 (d, J=8.2 Hz, 1H), 7.44-7.40 (m, 3H), 7.30 (d, J=8.4 Hz, 1H), 6.98 (d, J=8.7 Hz, 2H), 5.15 (s, 2H), 3.84 (s, 3H), 3.78 (s, 3H). MS (ES+, m/z)=273 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07491731B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-bb4d26a59a30453c927d395d4d645b4f |
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| Source note | uspto-grants-2009_02 |
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