HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990115Generated: November 1, 2026
1-Bromopropane → 4-Methoxy-3-propoxybenzaldehyde
https://huagongshe.com/reaction/990115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Isovanillin | HCID 12127 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Methoxy-3-propoxybenzaldehyde | HCID 592109 | 101.4% |
Reaction Steps
To a suspension of 3-hydroxy-4-methoxybenzaldehyde (2.00 g, 13.2 mmol), potassium carbonate (2.74 g, 19.8 mmol) and potassium iodide (60.0 mg, 0.361 mmol) in DMF (15 mL) was slowly added 1-bromopropane (1.56 mL, 17.2 mmol) via syringe. The reaction mixture was stirred at 65° C. for 5 hours. After cooling to room temperature, the mixture was diluted with diethyl ether (100 mL), and the organic phase was washed with water (2×50 mL). After drying over anhydrous MgSO4, filtration and evaporation of the filtrate in vacuo gave crude 3-(propyloxy)-4-methoxybenzaldehyde (2.60 g) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458829B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-04b024fa5deb4276ad84dc85be6ab684 |
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| Source note | uspto-grants-2002_10 |
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