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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422180Generated: November 2, 2026

Thionyl Chloride → 4-(1-Chloroethyl)-3-fluoro-pyridine

https://huagongshe.com/reaction/2422180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13129579HCID 13129579—
SolventWaterHCID 962—
Product4-(1-Chloroethyl)-3-fluoro-pyridineHCID 5824808039%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-(3-fluoropyridin-4-yl)ethanol (0.8 g, 5.7 mmol) was treated with thionyl chloride (5 mL) and the resulting mixture was heated to 80° C. for 2 h. Water (10 mL) and sat. sodium bicarbonate (aq., 10 mL) was added. The product was extracted with DCM (three times). The combined organic extracts were washed with brine, dried over sodium sulphate and concentrated in vacuo. The crude product was purified by flash column chromatography (eluent heptane: ethyl acetate gradient) to yield 0.36 g (39% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960395B2
Source datasetuspto-grants-2011_06
ORD IDord-e1eca158726246368a3227984f013933
Source noteuspto-grants-2011_06