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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618636Generated: November 1, 2026

Acetic Anhydride → 6-Bromo-1H-indole-3-carbonitrile

https://huagongshe.com/reaction/1618636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant6-Bromoindole-3-carbaldehydeHCID 2794830—
SolventPyridineHCID 1049—
Product6-Bromo-1H-indole-3-carbonitrileHCID 11470067—

Reaction Steps

To a solution of 6-bromo-1H-indole-3-carbaldehyde (1.2 g, 5.36 mmol) in pyridine (10 mL) was added NH2OH.HCl (0.424 g, 6.11 mmol) portionwise and the resulting mixture was stirred at rt for 1.5 h. 25 mL of Ac2O was added and the mixture was heated at reflux overnight. After this time the reaction mixture was cooled to rt and poured into ice. The resulting solid was filtered and the product was purified by flash column chromatography to give 6-bromo-1H-indole-3-carbonitrile slightly impure but was used for the next step. Mass Spectrum (ESI) m/e=222 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-1249dd06b51c4028ab2e8e0879b64549
Source noteuspto-grants-2014_07