Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Fluoropyridine | HCID 9746 | — |
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-((4-Bromobenzyl)oxy)pyridine | HCID 24799160 | 99% |
Reaction Steps
To a solution of 4-bromobenzyl alcohol (25 g, 130 mmol) in N,N-dimethylformamide (125 mL) was added potassium tert-butoxid at room temperature, which was stirred for 10 minutes at 54° C. To this reaction solution was added 2-fluoropyridine (15 mL, 154 mmol) at a temperature of from 40° C. to 58° C., which was stirred for another 30 minutes at 65° C. The reaction solution was cooled to room temperature, water and ethyl acetate were added to separate the reaction solution. The aqueous layer was further extracted (twice) with ethyl acetate. This was combined with an ethyl acetate layer, washed with water (three times) and saline (once), and was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under a reduced pressure. Diethyl ether was added to the residue, and this was concentrated under a reduced pressure, so as to obtain a crude product of the titled compound (34 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188119B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-ec9be5a30e994da99f383400a3633ded |
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| Source note | uspto-grants-2012_05 |
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