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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255571Generated: October 31, 2026

Acetone → 3-[4-(Bromomethyl)phenyl]2-phenylpropanonitrile

https://huagongshe.com/reaction/2255571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant3-[4-(Tert-butyldimethylsilyloxymethyl)phenyl]-2-phenylpropanonitrileHCID 19385650—
SolventAcetonitrileHCID 6342—
Product3-[4-(Bromomethyl)phenyl]2-phenylpropanonitrileHCID 1938559445%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of 1.5 g (4.27 mmol) of the product of Step C dissolved in 20 mL of acetonitrile, was added 2.12 g (6.4 mmol) of carbon tetrabromide, and 1.68 g (6.40 mmol) of triphenylphosphine. The reaction mixture was stirred 30 minutes at 0° C., then allowed to warm to room temperature and 0.5 mL (6.4 mmol) of acetone was added. The reaction mixture was stirred an additional 16 hours at room temperature, then filtered and evaporated in vacuo. The residue was purified on a silica gel flash chromatography column eluted with 5% ethyl acetate/hexane to afford 0.575 g (45%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240938
Source datasetuspto-grants-1993_08
ORD IDord-9164cf9c7bac4ac5b0fb1a755c16164e
Source noteuspto-grants-1993_08