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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255274Generated: November 1, 2026

Potassium Carbonate → 2-(3-Bromo-2-methylphenyl)ethan-1-ol

https://huagongshe.com/reaction/1255274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-3-(2-methoxyvinyl)-2-methylbenzeneHCID 66963736—
CatalystMercuric acetateHCID 15337—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Bromo-2-methylphenyl)ethan-1-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455483B2
Source datasetuspto-grants-2013_06
ORD IDord-db411f8c48904a238a1a98e861f78564
Source noteuspto-grants-2013_06