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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041732Generated: November 2, 2026

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

https://huagongshe.com/reaction/2041732

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 105) (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 min, 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 numberUS08580957B2
Source datasetuspto-grants-2013_11
ORD IDord-88c81fba31bf42388be2f855e92a9935
Source noteuspto-grants-2013_11