HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097470Generated: October 31, 2026
Dimethylformamide → 4-Bromo-2-cyclobutoxy-1-methoxybenzene
https://huagongshe.com/reaction/2097470
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-cyclobutoxyphenol | HCID 66602954 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromo-2-cyclobutoxy-1-methoxybenzene | HCID 58189113 | 59% |
Reaction Steps
To 60 ml of N,N-dimethylformamide solution containing 6.22 g (25.6 mmol) of 4-bromo-2-cyclobutoxyphenol obtained in Reference Example 5-(d) were successively added 3.54 g of potassium carbonate and 3.2 ml of methyl iodide, and the mixture was stirred at room temperature for 6 hours. After completion of the reaction, water was added to the reaction mixture, and the mixture was extracted with toluene. The organic layer after separation was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The obtained residue was applied to silica gel column chromatography (Eluent; toluene), and the obtained crude solid was recrystallized from hexane to obtain 3.90 g of the title compound as a colorless solid. (Yield: 59%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450319B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-4cd84fe83a1a4157b7fe9d1cfad5ecd5 |
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| Source note | uspto-grants-2013_05 |
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