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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-(4-(tert-Butyl)pyridin-2-yl)ethanolHCID 18799657—
SolventDichloromethaneHCID 6344—
Product4-t-Butyl-2-(1-chloroethyl)-pyridineHCID 1879992498.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043248
Source datasetuspto-grants-2000_03
ORD IDord-cbed1e7569cf48428cc4341d52a8c061
Source noteuspto-grants-2000_03