HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094808Generated: November 2, 2026
Methyl iodide → 2-Bromo-1-chloro-4-methoxymethyl-benzene
https://huagongshe.com/reaction/1094808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (3-Bromo-4-chlorophenyl)methanol | HCID 50998689 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-Bromo-1-chloro-4-methoxymethyl-benzene | HCID 57582345 | 94% |
Reaction Steps
To a stirred solution of 4-chloro-3-bromophenyl-methanol (cited in Amgen patent WO03099776) (900 mg, 4.06 mmol) in 2-methyl-tetrahydrofuran (15 ml) was added potassium hydroxide (912 mg, 16.3 mmol) and the resulting suspension was stirred at room temperature for 30 minutes. Iodomethane (1.01 ml, 4.00 mmol) was then added and the reaction was stirred for 16 hours at room temperature. LCMS indicated incomplete reaction. Potassium hydroxide (912 mg, 16.3 mmol) was added and the resulting mixture stirred for 5 minutes before adding further iodomethane (4.04 ml, 16 mmol) and stirring was continued for 3 hours at room temperature. Ethyl acetate (60 ml) and saturated brine solution (30 ml) were added and the layers were separated. The organic extract was further washed with saturated brine solution (2×30 ml) then dried over anhydrous MgSO4 (s), filtered and evaporated in vacuo to afford the crude title compound as a yellow oil (901 mg, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134007B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-267179f55ba24baf8b8fa5d39c8a28d4 |
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| Source note | uspto-grants-2012_03 |
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