HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850478Generated: October 25, 2026
Dimethylformamide → 2-Bromo-4-methoxy-3-(pentyloxy)benzaldehyde
https://huagongshe.com/reaction/850478
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromoisovanillin | HCID 224011 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-4-methoxy-3-(pentyloxy)benzaldehyde | HCID 19363349 | — |
Reaction Steps
2-Bromo-3-hydroxy-4-methoxybenzaldehyde (225.2 g, 975 mmol) and DMF (660 ml) were mixed, and potassium carbonate (148.2 g, 1.07 mol) and bromopentane (133 ml, 1.07 mol) were successively added to this solution. The mixture was stirred at 90° C. for 1.5 hours and cooled to room temperature. Water (800 ml) was added to stop the reaction. The aqueous layer was extracted successively with diethyl ether (1000 ml, 500 ml) and ethyl acetate (500 ml). The organic layers were combined, washed successively with water (200 ml) and saturated brine (200 ml) and dried over anhydrous sodium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure to give a crude product of 2-bromo4-methoxy-3-pentyloxybenzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017919 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-d2c96e3b5092473cb15a8c3dafb1c06d |
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| Source note | uspto-grants-2000_01 |
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