HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874311Generated: November 3, 2026
Benzyl Bromide → 4-Benzyloxyphenylacetonitrile
https://huagongshe.com/reaction/1874311
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxybenzyl cyanide | HCID 26548 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxyphenylacetonitrile | HCID 522804 | 77.8% |
Reaction Steps
Acetone (500 ml) and potassium carbonate (154 g) were charged into RB flask followed by addition of p-hydroxy phenyl acetonitrile (100 g) under stirring. Benzyl bromide (154 g) was then added at ambient temperature, subsequently heating the reaction mass to 55-58° C. and maintaining for 2 hours. The reaction mass was then cooled to 25° C., filtered and washed with acetone (100 ml) to give 130 g (77.8%) of the p-benzyloxyphenyl acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304578B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-62e7be9475384d7b9a34de7c77006b95 |
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| Source note | uspto-grants-2012_11 |
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