HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922258Generated: October 25, 2026
Methyl iodide → 4-Benzyloxy-2-methoxybenzaldehyde
https://huagongshe.com/reaction/922258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzyloxy-2-hydroxybenzaldehyde | HCID 561235 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Benzyloxy-2-methoxybenzaldehyde | HCID 4293990 | 100% |
Reaction Steps
To a 100 mL RB flask fitted with magnetic stirrer was charged with 10 mL of acetonitrile. To the stirred solvent were added 4-(benzyloxy)-2-hydroxybenzaldehyde (1.0 g, 4.38 mmol), potassium carbonate (1.21 g, 8.76 mmol). The reaction mixture was brought to 0° C., was added methyl iodide (1.135 g, 8.76 mmol) in acetonitrile (5 mL) drop wise and stirred at room temperature for 16 h. The reaction mixture was concentrated to distill off the solvent. The residue was extracted with ethyl acetate (50 mL). The organic layer was washed with water (40 mL) and saturated brine solution (40 mL). The organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The product obtained as a white solid (1.06 g, yield: 100.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278915B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-7bde54a000014bf58f71b87d9aeae0e5 |
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| Source note | uspto-grants-2016_03 |
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