HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556177Generated: October 31, 2026
Dimethyl Sulfate → 5-Bromo-1,3-di-tert-butyl-2-methoxybenzene
https://huagongshe.com/reaction/556177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2,6-di-tert-butylphenol | HCID 70829 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Bromo-1,3-di-tert-butyl-2-methoxybenzene | HCID 13691541 | 106.9% |
Reaction Steps
Under an argon atmosphere, to a solution of 4-bromo-2,6-di-tert-butylphenol (50 g, 0.175 moL) and potassium carbonate (96.7 g, 4.0 equivalents) in acetone (750 mL) was added dimethyl sulfate (38.6 g, 1.75 equivalents) at 22° C., and the mixture was stirred under reflux for 13 hrs. Insoluble materials were filtered off and the solvent was evaporated under reduced pressure. Ethylacetate (150 mL) and water (100 mL) were added, the mixture was partitioned, and the organic layer was washed successively with water (100 mL), 5% aqueous NaHCO3 solution (100 mL) and 5% aqueous NaCl solution (100 mL). The organic layer was dried over anhydrous magnesium sulfate, filtered by gravity, and the filtrate was concentrated under reduced pressure to give the title compound (56.1 g, brown oil). yield 95.2%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053604B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-8b3e9b986e7d4abf83d18d0e3293ed86 |
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| Source note | uspto-grants-2011_11 |
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