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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084449Generated: October 29, 2026

Oxalyl chloride → HCID 20063329, compound

https://huagongshe.com/reaction/1084449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 19778163HCID 19778163—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20063329HCID 20063329—

Reaction Steps

A solution of (E)-3-[4-(4-fluorophenyl)-2-isopropyl-1-oxo-1,2-dihydroisoquinolin-3-yl]prop-2-enoic acid (0.35 g) in dry tetrahydrofuran (10 ml) was treated with oxalyl chloride (0.26 ml) and heated at reflux for 2 hours. The solvent was then removed by distillation and the residual yellow solid was washed with petroleum ether (b.p. 40°-60° C.), to give (E)-3-[4-(4-fluorophenyl)-2-isopropyl-1-oxo-1,2-dihydroisoquinolin-3-yl]prop-2-enoyl chloride in the form of a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004747
Source datasetuspto-grants-1991_04
ORD IDord-7389806d9221485b82aa504164296330
Source noteuspto-grants-1991_04