Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluorophenol | HCID 9707 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(Chloromethyl)quinoline hydrochloride | HCID 3083823 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14097601 | HCID 14097601 | 53% |
Reaction Steps
To a solution of 2-fluorophenol (7.8 g, 70 mmol) in 20 mL ethanol is added 2-(chloromethyl)quinoline hydrochloride (15.0 g, 70 mmol) followed by a solution of potassium hydroxide (7.86 g, 140 mmol) in 50 mL ethanol. The reaction mixture is refluxed overnight. After filtering while still hot, the reaction mixture is cooled to 8° C. to afford 9.3 g (53%) of brown crystals, m.p. 84°-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04732978 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-001cfba669ba4eedaf3c1bab5435b846 |
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| Source note | uspto-grants-1988_03 |
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