HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253402Generated: October 30, 2026
Methyl iodide → 2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzene
https://huagongshe.com/reaction/2253402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (4-Bromo-3,5-dimethoxyphenyl)methanol | HCID 11149289 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzene | HCID 23080940 | — |
Reaction Steps
Sodium hydride (60% in oil; 24.7 g) was added to a solution of (4-bromo-3,5-dimethoxyphenyl)methanol (118.8 g) in N,N-dimethylformamide (960 mL) while cooling with ice, and after stirring for 10 minutes, iodomethane (41.7 mL) was added dropwise, the temperature was increased to room temperature and stirring was continued for 1 hour. The obtained reaction mixture was poured into ice water (2.5 L), extraction was performed with ethyl acetate, the extract was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and the title compound (121.3 g) was obtained as a colorless oil from the n-hexane:ethyl acetate (4:1) fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323569B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-9611bc61c2bf4609a9047e035150afa1 |
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| Source note | uspto-grants-2008_01 |
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