Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604623Generated: November 2, 2026

Acetic Anhydride → 5-Methyl-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/1604623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Methylindole-3-carboxaldehydeHCID 259187—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product5-Methyl-1H-indole-3-carbonitrileHCID 1960373122.2%

Reaction Steps

A mixture of 3-formyl-5-methylindole (0.50 g), hydroxylamine hydrochloride (0.44 g) and sodium acetate (0.52 g) in acetic acid (5 ml) was stirred for 2 hours, then acetic anhydride (2.5 ml) was added to the mixture and allowed to react under reflux for 0.5 hour. After cooling, the reaction mixture was poured into ice-water and extracted with ethyl acetate. After filtration of insoluble materials, the filtrate was washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The resulting residue was subjected to column chromatography on silica gel and eluted with a mixture of ethyl acetate and chloroform. The fractions containing the objective compounds were combined and concentrated under reduced pressure to give 3-cyano-5-methylindole (109 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-73dd3509f3ba495fadf7846ef73e1851
Source noteuspto-grants-1999_11