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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722380Generated: November 1, 2026

Pyridine → 1-Chloro-5-ethoxyheptane

https://huagongshe.com/reaction/1722380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant5-EthoxyheptanolHCID 15053038—
SolventWaterHCID 962—
Product1-Chloro-5-ethoxyheptaneHCID 13924081—

Reaction Steps

The starting material prepared in Example 37, 5-ethoxyheptanol (238 g, 1.49 moles) is diluted in pyridine (128 g, 1.62 moles). The solution is stirred at room temperature and thionyl chloride (388 g, 3.22 moles) is added dropwise over 2 hours, after which time the reaction is heated in a 70° C. water bath for 2 additional hours. Water (700 ml) is added to the reaction and the organic layer separated. The aqueous layer is extracted with hexane (3×400 ml) and the extracts combined with the organic phase. The organic phase is then washed with a 10% sodium hydroxide solution (1000 ml). The solvent volume is reduced under vacuum and the residue dried over anhydrous magnesium sulfate. The remaining solvent is removed leaving a clear light yellow oil. The crude product is fractionally distilled under reduced pressure leaving a clear, colorless oil (162 g, 1.13 moles), BP 96° C./9.5 cm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855322
Source datasetuspto-grants-1989_08
ORD IDord-58621c17a5134b9b8d83dec7ad94a4ea
Source noteuspto-grants-1989_08