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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265953Generated: October 25, 2026

N-bromobutanimide → (3-(Bromomethyl)phenyl)trimethylsilane

https://huagongshe.com/reaction/1265953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantTrimethyl(M-tolyl)silaneHCID 10866684—
CatalystAzobisisobutyronitrileHCID 6547—
SolventChlorobenzeneHCID 7964—
Product(3-(Bromomethyl)phenyl)trimethylsilaneHCID 1258397799.1%

Reaction Steps

A mixture of m-trimethylsilyltoluene (8.22 g, 50 mmol), NBS (8.90 g, 50 mmol), AIBN (0.05 g) and chlorobenzene (50 ml) was heated by means of a heating bath preheated to 110° C. An exothermic reaction started when the reaction mixture reached 80-90° C. and the orange suspension became a colorless solution within minutes. The mixture was cooled down with the aid of an ice-bath, ice water was added and the resulting mixture was extracted with hexane. The organic phase was washed with water, then brine and dried (MgSO4). Filtration through a silica plug (10 g) followed by evaporation of solvents yielded 12.05 g (99%) of 37 as a colorless liquid. Spectroscopic data were identical to those reported in the literature.43

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548042B2
Source datasetuspto-grants-2003_04
ORD IDord-b9a1c361dc1743b78a88c1f5d3b418a9
Source noteuspto-grants-2003_04