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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989815Generated: October 27, 2026

N-bromobutanimide → 2-(3-Bromo-4-methoxyphenyl)-2-methylpropionitrile

https://huagongshe.com/reaction/1989815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 219166—
SolventTrifluoroacetic acidHCID 6422—
Product2-(3-Bromo-4-methoxyphenyl)-2-methylpropionitrileHCID 11368810—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(4-methoxy-phenyl)-2-methyl-propionitrile (17.5 g, 0.10 mol) in TFA (80 mL) was cooled to 0° C. N-bromosuccinimide (17.8 g, 0.10 mol) was added in small portions keeping the temperature below 5° C. The orange solution was stirred for 2 h/25° C. and evaporated to dryness. Water (200 mL) was added and the mixture was stirred vigorously for 1 h. The crude product was filtered off and recrystallized from boiling MeOH. The pure product was isolated as white needles. Yield: 19.3 g (76%). GCMS: >99%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642367B2
Source datasetuspto-grants-2010_01
ORD IDord-c9ede26dd7b74975a1adf6732b5b16f1
Source noteuspto-grants-2010_01