HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637732Generated: November 1, 2026
Thionyl Chloride → 4-t-Butyl-2-(1-chloroethyl)-pyridine
https://huagongshe.com/reaction/1637732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(4-(tert-Butyl)pyridin-2-yl)ethanol | HCID 18799657 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-t-Butyl-2-(1-chloroethyl)-pyridine | HCID 18799924 | 98.1% |
Reaction Steps
4-t-Butyl-2-(1-hydroxyethyl)-pyridine (3.6 g, 20.1 mmole) is dissolved in 60 ml dichloromethane in a 200 ml one neck round bottom flask under nitrogen. The solution is cooled to 0° C., is treated with thionyl chloride (2.2 ml, 30 mmole) in 10 ml dichloromethane, and the reaction is stirred 1 h at 0° C. followed by 2 h at room temperature. The reaction is quenched with 1×75 ml saturated sodium bicarbonate, the layers are separated and the aqueous layer is extracted with 3×25 ml dichloromethane. The combined organics are dried over potassium carbonate and are concentrated in vacuo to give 3.9 g (98%) of 4-t-Butyl-2-(1-chloroethyl)-pyridine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06043248 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-cbed1e7569cf48428cc4341d52a8c061 |
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| Source note | uspto-grants-2000_03 |
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