HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212141Generated: October 31, 2026
3,5-Dimethoxyphenol → HCID 21964056, compound
https://huagongshe.com/reaction/2212141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dimethoxyphenol | HCID 10383 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,5-Dibromopyridine | HCID 69369 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21964056 | HCID 21964056 | 98.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101896B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-19e9fb7ec28845bf9fd4be6d942bd712 |
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| Source note | uspto-grants-2006_09 |
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