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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743162Generated: October 27, 2026

Ethanol → 2-chloro-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/743162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPyridineHCID 1049—
Reactant2-chloro-1H-indole-3-carbaldehydeHCID 314791—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventWaterHCID 962—
SolventAcetic AnhydrideHCID 7918—
Product2-chloro-1H-indole-3-carbonitrileHCID 1032985458%

Reaction Steps

A mixture of 2-chloroindole -3-carboxaldehyde (7.0 g, 36 mmol) was reacted with a slight excess of hydroxylamine hydrochloride and pyridine in refluxing EtOH for 1 hour, to give the crude oxime (Latrell R, Bartmann W, Musif J, Granzer E, German Patent 2,707,268, 31 Aug. 1978, Chem. Abstr. 1978;89:179858y). A solution of this in Ac2O (100 mL) was heated under reflux for 1 hour, cooled, and stirred with water (700 mL). The precipitated solid was collected, washed with water, and crystallized from aqueous MeOH to give 2-chloro-1H-indole-3-carbonitrile (3.7 g, 58%); mp 177°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556874
Source datasetuspto-grants-1996_09
ORD IDord-c2ded592d5b14f6ab97eb06604609361
Source noteuspto-grants-1996_09