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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399462Generated: October 31, 2026

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

https://huagongshe.com/reaction/2399462

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 numberUS05449682
Source datasetuspto-grants-1995_09
ORD IDord-c977ffe473024735afeae4c81b711010
Source noteuspto-grants-1995_09