HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884568Generated: October 27, 2026
Ethylene Oxide → 3-(3-Cyanopyridin-4-yl)-1-propanol
https://huagongshe.com/reaction/1884568
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Methyl-3-cyanopyridine | HCID 227806 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3-Cyanopyridin-4-yl)-1-propanol | HCID 23506213 | 37% |
Reaction Steps
Diisopropylamine (2.5 g, 25 mmol) is dissolved in THF (30 ml), and thereto is added a solution of n-butyl lithium in hexane (14.3 ml, 24 mmol) at −70° C. The mixture is stirred for 15 minutes, and thereto is added a solution of 3-cyano-4-methylpyridine (2.4 g, 20 mmol) obtained in Reference Example 33 in THF (20 ml). Ten minutes thereafter, ethylene oxide (1.1 g, 24 mmol) is added to the mixture, and the mixture is warmed to 20° C. over a period of time for one hour. The reaction is quenched with a saturated brine (50 ml), and the mixture is extracted with ethyl acetate (150 ml×2). The organic layer is washed with a saturated brine (100 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to give the title compound (1.2 g) as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06765095B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-e923d8275ae84c76895826e506133f03 |
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| Source note | uspto-grants-2004_07 |
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