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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-[4-(Tert-butyldimethylsilyloxymethyl)phenyl]-2-phenylpropanonitrile | HCID 19385650 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-[4-(Bromomethyl)phenyl]2-phenylpropanonitrile | HCID 19385594 | 45% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05240938 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-9164cf9c7bac4ac5b0fb1a755c16164e |
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| Source note | uspto-grants-1993_08 |
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