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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814588Generated: October 26, 2026

2-Cyanobenzeneacetonitrile → 1-Bromoisoquinolin-3-amine

https://huagongshe.com/reaction/1814588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-CyanobenzeneacetonitrileHCID 77368—
ReactantHydrogen bromide acetateHCID 20344520—
SolventAcetic AcidHCID 176—
Product1-Bromoisoquinolin-3-amineHCID 28984590.8%

Reaction Steps

To a suspension of α-cyanotolunitrile (20.0 g) in acetic acid (50 ml) was added 25% hydrogen bromide/acetate solution (150 ml), and the mixture was reacted at room temperature overnight. The resulting precipitates were collected by filtration and then added to a 10% aqueous solution of potassium carbonate. The yellow powder was changed to a pale yellow powder. The resulting powder was collected by filtration, washed with water and hexane, and dried at 50° C. under reduced pressure, to give 3-amino-1-bromoisoquinoline (28.5 g; 90.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-7cbcd151018848d4b441dbf2af787954
Source noteuspto-grants-2005_04