HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161763Generated: October 27, 2026
Methyl iodide → 2,6-Dichloro-4-methoxybenzaldehyde
https://huagongshe.com/reaction/1161763
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dichloro-4-hydroxybenzaldehyde | HCID 528382 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,6-Dichloro-4-methoxybenzaldehyde | HCID 14771759 | — |
Reaction Steps
Combine 2,6-dichloro-4-hydroxy-benzaldehyde (120 g, 628.24 mmol) and potassium carbonate (173.65 g, 1256.5 mmol) in 900 mL dimethylformamide and treat with iodomethane (107 g, 753.9 mmol). Stir the reaction at room temperature for 3 hours. Filter off solids and pour into 6 L of water. Filter solids, wash several times with water, air dry and dissolve in ethyl acetate. Wash with water, followed by brine and then dry over sodium sulfate. Filter and concentrate under vacuum to 100 mL volume, at which point, solids start to crash out. Filter then concentrate down the filtrate to yield a second crop. Wash with hexane, combine all solids and vacuum dry to yield 112.3 g of off-white, solid: 1H NMR (400 MHz, CDCl3) δ 10.41 (s, 1H), 6.90 (s, 2H), 3.87 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820659B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-10d5d08843fc44d892b58b49d9186fff |
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| Source note | uspto-grants-2010_10 |
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