HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77633Generated: October 25, 2026
Vanillin → 3-Methoxy-4-(methoxymethoxy)benzaldehyde
https://huagongshe.com/reaction/77633
Participants
| Role | Name | HCID | Charge |
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| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxy-4-(methoxymethoxy)benzaldehyde | HCID 79661 | 99.2% |
Reaction Steps
4-Hydroxy-3-methoxybenzaldehyde (1a, 2.00 g, 13.1 mmol) and potassium carbonate (9.00 g, 65.1 mmol) were combined in dimethyl formamide (30 ml) and stirred for 15 min at room temperature. Chloromethyl methyl ether (1.60 ml, 21.1 mmol) was added and stirring was continued for 6 hr at room temperature. The resulting mixture was filtered and the filtrate extracted into ethyl acetate, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to give 2.55 g (99%) of a white solid: mp 39-40° C. [expected mp 41° C.]; 1H NMR: δ 3.40 (s, 3H), 3.83 (s, 3H), 5.21 (s, 2H), 7.15 (d, 1H, J=8.7 Hz), 7.30 (dd, 1H, J=6.0, 2.0 Hz), 7.32 (s, 1H), 9.75 (s, 1H); 13C NMR: δ 55.8, 56.2, 94.8, 109.4, 114.6, 125.9, 130.9, 149.8, 151.7, 190.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841326B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-0ad326e1fe4b4d149bf0bbc0b8d9d86c |
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| Source note | uspto-grants-2014_09 |
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