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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603205Generated: October 31, 2026

4-Aminobenzonitrile → 213978-36-0

https://huagongshe.com/reaction/1603205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzonitrileHCID 13396—
ReactantSodium HydroxideHCID 14798—
Reactant1719-99-9HCID 11032746—
SolventAcetonitrileHCID 6342—
Product213978-36-0HCID 9860086—

Reaction Steps

2-Bromo4-chlorobutyryl bromide (BCBB, 145.7 g, 0.540 mole) was added via an addition funnel to a cold (5° C.), well stirred slurry of 4-aminobenzonitrile (4-ABN, 55.0 g, 0.466 mole), Na3PO4 (42 g, 0.256 mole) and acetonitrile (550 mL) in a 1 liter flask while maintaining a temperature below 30° C. during the addition. The addition funnel was rinsed with acetonitrile (55 mL). Upon completion of the coupling (determined by LC), a 50 wt % solution of NaOH (56 mL, 1.061 mole) was added via an addition funnel while maintaining the reaction temperature below 30° C. Upon completion of the reaction (determined by LC), the slurry was filtered through a pressure filter (10 micron polypropylene filter cloth). The flask and the cake were washed with acetonitrile (256 mL). The filtrate and the wash were combined to afford a solution of 4-(3-bromo-2-oxopyrrolidin-1-yl)benzonitrile in acetonitrile (of about 17 wt %). Qualitative LC analysis showed the product with 91.8 to 95 area % purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05986107
Source datasetuspto-grants-1999_11
ORD IDord-44bceb09cfc547dea5c4fb221191bf8d
Source noteuspto-grants-1999_11