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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212141Generated: October 31, 2026

3,5-Dimethoxyphenol → HCID 21964056, compound

https://huagongshe.com/reaction/2212141

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DimethoxyphenolHCID 10383—
ReactantSodium hydrideHCID 24758—
Reactant3,5-DibromopyridineHCID 69369—
SolventDimethylformamideHCID 6228—
ProductHCID 21964056HCID 2196405698.9%

Reaction Steps

Under an argon atmosphere, a solution of 3,5-dimethoxyphenol (6.94 g, 45 mmol) in dimethylformamide (30 mL) was added slowly to a stirred suspension of sodium hydride (1.44 g of a 75% suspension in mineral oil, 0.045 mol) in dimethylformamide (30 mL) at 0–5° C. The icebath was removed and the resulting mixture was stirred for 2.5 h at room temperature. 3,5-Dibromopyridine (7.11 g, 0.03 mol) was added to the mixture, which was then heated to 100° C. for 72 h, then the mixture was cooled to room temperature and successively washed with water (100 mL) and 5 N NaOH solution (10 mL). The mixture was extracted with diethyl ether (3×50 mL). The combined organic phases were dried (MgSO4), filtered and concentrated by rotary evaporation to give 9.2 g of a white solid, which was purified by column chromatography, eluting with cyclohexane/ethyl acetate (90/10, v/v). Selected fractions containing the product were concentrated via rotary evaporation to give 2.5 g (29%) of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101896B2
Source datasetuspto-grants-2006_09
ORD IDord-19e9fb7ec28845bf9fd4be6d942bd712
Source noteuspto-grants-2006_09