HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741590Generated: November 1, 2026
3-Fluorophenol → 2-Cyano-3-(3-fluorophenoxymethyl)pyridine
https://huagongshe.com/reaction/1741590
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluorophenol | HCID 9743 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3-(Bromomethyl)pyridine-2-carbonitrile | HCID 10375450 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Cyano-3-(3-fluorophenoxymethyl)pyridine | HCID 10263162 | — |
Reaction Steps
To a chilled solution of sodium ethoxide, prepared from 13.8 g of sodium metal and 240 ml of absolute ethanol, 56.9 ml of 3-fluorophenol was added and the mixture was stirred at room temperature for 30 minutes. Crude 3-bromomethyl-2-cyanopyridine (103 g) was added to the mixture at 5° C., and the mixture was reflexed for 2 hours. After being concentrated, the reaction mixture was diluted with ether, and the resultant insoluble materials were removed by filtration. The filtrate was washed with 10% aqueous sodium hydroxide solution and with water, dried over anhydrous sodium sulfate, and then concentrated. The residue was crystallized by trituration with a mixture of ether and n-hexane to yield 58.0 g of pale brown crystals, which were recrystallized from isopropyl ether to give pale yellow needles, mp 52°-53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05334594 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-32e8dcd982d54917ba69b9a170485f54 |
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| Source note | uspto-grants-1994_08 |
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