HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510580Generated: October 27, 2026
Methyl iodide → 2,4-Dichloro-6-methoxybenzaldehyde
https://huagongshe.com/reaction/510580
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dichloro-6-hydroxybenzaldehyde | HCID 528390 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,4-Dichloro-6-methoxybenzaldehyde | HCID 12802880 | 97% |
Reaction Steps
To a stirred solution of 2,4-dichloro-6-hydroxybenzaldehyde (1.85 g; 9.7 mmol) in 20 mL DMF at ambient temperature was added solid potassium carbonate (1.47 g; 10.6 mmol), and the resulting yellow mixture was stirred at ambient temperature. After 30 minutes, iodomethane (5.5 g; 38.7 mmol) was added, and the resulting mixture was stirred in an oil bath set to 50° C. After 10 minutes, the reaction was determined to be complete by thin layer chromatography (90/10 hexane/EtOAc). After a total of 30 minutes the mixture was cooled to ambient temperature and diluted with 200 mL water. After stirring for a few minutes, the precipitate that formed was collected by filtration, washed with water, and dried under vacuum to give 1.93 g of 2,4-dichloro-6-methoxybenzaldehyde as an off-white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096567B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-44116caff36948248b3e39539183be09 |
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| Source note | uspto-grants-2015_08 |
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