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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366844Generated: October 30, 2026

N-bromobutanimide → (3S)-3-[(4-bromophenyl)amino]butanenitrile

https://huagongshe.com/reaction/2366844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant(3S)-3-(phenylamino)butanenitrileHCID 39235654—
SolventDimethylformamideHCID 6228—
Product(3S)-3-[(4-bromophenyl)amino]butanenitrileHCID 67173345—

Reaction Steps

(3S)-3-(phenylamino)butanenitrile (for a preparation see Intermediate 31) (11.3526 g, 70.9 mmol) was taken up in N,N-dimethylformamide (DMF) (200 mL) under nitrogen and cooled in an ice-bath. NBS (12.61 g, 70.9 mmol) was added and the reaction stirred. After 20 mins, the reaction was partitioned between EtOAc (1000 ml) and water (500 ml). The organic layer was washed with 2M NaOH ×2, water and brine (500 ml each) and then dried with Na2SO4, filtered and concentrated to yield the product as a cream solid (17.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697725B2
Source datasetuspto-grants-2014_04
ORD IDord-455e9dd361ef4685b218048b41dba8ea
Source noteuspto-grants-2014_04