HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271699Generated: October 26, 2026
Diethyl Ether → 5-Fluoro-2-methylpyridine 1-oxide
https://huagongshe.com/reaction/1271699
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Butyl nitrite | HCID 10996 | — |
| Reactant | 5-Amino-2-methylpyridine | HCID 243313 | — |
| Reactant | 5-Fluoro-2-methylpyridine | HCID 2762863 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrafluoroboric acid | HCID 28118 | — |
| Product | 5-Fluoro-2-methylpyridine 1-oxide | HCID 19691306 | — |
Reaction Steps
Preparation of 5-fluoro-2-picoline was based on E. J. Blanz, F. A. French, J. R. DoAmaral and D. A. French, J. Med. Chem. 1970, 13, 1124–1130. 5-Amino-2-picoline (12.5 g) in ethanol (105 ml) and 50% fluoroboric acid (44.5 ml) was stirred at −5° C. and treated dropwise over 45 mins. with n-butyl nitrite (31.25 ml). The solution was maintained at this temp. for 3 hours, treated with ether (100 ml, precooled to −20° C.) and the solid filtered off, quickly transferred to a flask and covered with hexane (precooled to −20° C.). After allowing to warm to approx. 20° C. and standing for 3 days the hexane was decanted and 2M NaOH solution added until basic (pH10). The mixture was filtered and the filtrate extracted with dichloromethane (10×200 ml). The organic solution was dried, evaporated to 200 ml and treated with m-chloroperbenzoic acid (26.5 g). After stirring 16 hours the solution was washed with excess aqueous sodium bicarbonate and the aqueous re-extracted with dichloromethane (10×200 ml). The organic fraction was dried and evaporated and the residue chromatographed (15% EtOH/EtOAc) to give the product (5.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205408B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-5d00d9c2d8cf43169e209aee62c92684 |
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| Source note | uspto-grants-2007_04 |
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