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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073319Generated: October 31, 2026

Thionyl Chloride → (E)-4-(4-chloro-1-butenyl)isoquinoline

https://huagongshe.com/reaction/2073319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(E)-4-(4-isoquinolinyl)-3-buten-1-olHCID 14750832—
SolventChloroformHCID 6212—
Product(E)-4-(4-chloro-1-butenyl)isoquinolineHCID 14750833—

Reaction Steps

A solution of 3.3 g of (E)-4-(4-isoquinolinyl)-3-buten-1-ol in 15 mL of dry chloroform was added to a cold solution of 1.8 mL of thionyl chloride in 5 mL of dry chloroform. After 15 minutes, the cooling bath was removed and the reaction was stirred at room temperature for 1 hour and then at reflux for 3 hours. The cooled mixture was washed with NaHCO3 solution and with brine then was dried (Na2SO4) and evaporated. The residue was purified by chromatography over silica gel (ethyl acetate-toluene; 3:17) to yield 2.2 g of (E)-4-(4-chloro-1-butenyl)isoquinoline as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04916145
Source datasetuspto-grants-1990_04
ORD IDord-8739ed825a2f4ea1a068edbe08a91bca
Source noteuspto-grants-1990_04