HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425822Generated: October 30, 2026
Methyl iodide → 2-Bromo-5-methoxy-1,3-dimethylbenzene
https://huagongshe.com/reaction/2425822
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-3,5-dimethylphenol | HCID 81970 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Bromo-5-methoxy-1,3-dimethylbenzene | HCID 235992 | 99% |
Reaction Steps
To a mixture of 4-bromo-3,5-dimethyl-phenol (40.2 g, 0.200 mol) and potassium carbonate (55.2 g, 0.400 mol) in acetone (200 mL) was added methyl iodide (24.9 mL, 0.600 mol) at room temperature under N2. The reaction mixture was then refluxed at 65° C. for 8 h. After cooling to room temperature, the mixture was filtered, and the filtrate was concentrated in vacuo. The resulting clear liquid was distilled under reduced pressure (70° C./0.1 Torr) to give 42.4 g (99%) of title compound as a colorless liquid. 1H NMR (400 MHz, CDCl3): δ 6.663 (s, 2H), 3.778 (s, 3H), 2.402 (s, 6H); 13C NMR (100 MHz, CDCl3): δ 158.165, 139.203, 118.357, 113.953, 55.520, 24.319. MS (EI): m/z 214 [M+, 79Br 100], 216 [M+, 79Br, 96].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968016B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-f42b26049b734b0a89274adb635c91b2 |
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| Source note | uspto-grants-2011_06 |
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