Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21477477 | HCID 21477477 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21477483 | HCID 21477483 | — |
Reaction Steps
Thionyl chloride (1.03 ml) is added to 4-pyridinehexanol hydrochloride (2.42 g) and the mixture is stirred at 20° C. for 30 minutes. Excess saturated aqueous NaHCOs and CHCl3 (20 ml) is added. The organic phase is washed with saturated NaHCO3, brine and water, dried (MgSO4) and the solvent evaporated to give crude material which is purified by flash chromatography on silica gel (CH3OH:CHCl3 =1:49 by vol.) to give 4-(6-chlorohexyl)-pyridine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686564 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-86ecff1e3e3a4a0aaecdf2cf0eca3328 |
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| Source note | uspto-grants-1997_11 |
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