HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820697Generated: October 29, 2026
Water → 1-Bromo-3-(4-methoxybenzyloxy)-2-methylbenzene
https://huagongshe.com/reaction/1820697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methoxybenzyl alcohol | HCID 7738 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromo-6-fluorotoluene | HCID 2736335 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Heptane | HCID 8900 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 1-Bromo-3-(4-methoxybenzyloxy)-2-methylbenzene | HCID 66881855 | 46% |
Reaction Steps
1-Bromo-3-fluoro-2-methylbenzene (388 mg, 2.05 mmol), and (4-methoxyphenyl)methanol (0.511 mL, 4 mmol) were dissolved in DMF (5 mL) in a microwave vessel. Sodium hydride as a 60% dispersion in mineral oil (164 mg, 4.0 mmol) was added portionwise under a flow of nitrogen over 10 min. The reaction vessel was then sealed and heated at 180° C. for 900s. The crude reaction mixture was poured onto 1:1 water:brine (6 mL) and DCM (10 mL). The biphasic mixture was stirred at ambient temperature for 1 h and then the organic and aqueous layers were separated. The combined organics were dried over Na2SO4 and concentrated in vacuo. The crude material was then purified by chromatography on silica gel. Elution with 5:95 ethyl acetate:heptane afforded 1-bromo-3-(4-methoxybenzyloxy)-2-methylbenzene (289 mg, 0.9 mmol, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605170B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-dc8c987f83e246a5a1e324424767899d |
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| Source note | uspto-grants-2009_10 |
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