HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446398Generated: October 30, 2026
Potassium Carbonate → 2-(3-Bromo-2-methylphenyl)ethan-1-ol
https://huagongshe.com/reaction/446398
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-3-(2-methoxyvinyl)-2-methylbenzene | HCID 66963736 | — |
| Catalyst | Mercuric acetate | HCID 15337 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Bromo-2-methylphenyl)ethan-1-ol | HCID 58168541 | — |
Reaction Steps
To an ice-cold solution of 1-bromo-3-(2-methoxyvinyl)-2-methylbenzene [Aromatic Intermediate 22, step a] (1.75 g) in THF (25 mL) was added a solution of mercury(II) acetate (2.95 g) in water (30 mL) and the resulting solution was stirred in ice-water for 2.75 hours. Meanwhile, potassium carbonate (35 g) was dissolved in water (30 mL) and the solution was filtered. Sodium borohydride (1.17 g) was part dissolved/part suspended in 35 mL of the resulting potassium carbonate solution, and added to the reaction mixture from above. A grey, cloudy, two-phase mixture was formed, that was stirred at room temperature for 2.5 hours, then poured into water and extracted twice with ethyl acetate. The combined organic phases were washed with brine, dried (MgSO4), filtered and concentrated in vacuo to afford the subtitled compound as a colourless oil. Yield 1.67 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476265B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-0e99c0e2e8f548b1a6fb9f6ef9c16959 |
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| Source note | uspto-grants-2013_07 |
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