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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611404Generated: October 30, 2026

Oxalyl chloride → 2-(1-(4-chlorobenzyl)-1H-indol-3-yl)-2-oxo-acetyl chloride

https://huagongshe.com/reaction/1611404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1-(4-Chlorobenzyl)-1h-indoleHCID 967163—
SolventDiethyl EtherHCID 3283—
Product2-(1-(4-chlorobenzyl)-1H-indol-3-yl)-2-oxo-acetyl chlorideHCID 10980477—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1-(4-chlorobenzyl)-1H-indole (2.0 g) in dry ethyl ether (5 ml) kept under stirring and cooled at 0° C. is dropwise added with a solution of oxalyl chloride (0.85 ml) in dry ethyl ether (2 ml). After completion of the addition, the mixture is left at room temperature for 2h. The separated solid is recovered by filtration, washed with dry ethyl ether and dried under vacuum at 40° C. to give 2-(1-(4-chlorobenzyl)-1H-indol-3-yl)-2-oxo-acetyl chloride (1.64 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987122B2
Source datasetuspto-grants-2006_01
ORD IDord-f2c332d715d34f19be366fad1dc67ea6
Source noteuspto-grants-2006_01