HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657967Generated: October 25, 2026
Water → Benzeneacetonitrile, 4-(2,2-dimethyl-1-oxopropyl)-
https://huagongshe.com/reaction/1657967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-[4-(Bromomethyl)phenyl]-2,2-dimethylpropan-1-one | HCID 12831007 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzeneacetonitrile, 4-(2,2-dimethyl-1-oxopropyl)- | HCID 4341141 | — |
Reaction Steps
A solution of 34.3 g. (0.700 mole) sodium cyanide in 40 ml. of water is warmed to 50°C. and a solution of α-bromo-4-pivaloyl toluene in 85 ml. ethanol is then added dropwise at such a rate as to maintain the temperature at 50°C. After the addition is complete, the mixture is refluxed for four hours. The excess ethanol is removed in vacuo and the resulting residue is treated with ether/water. The layers are separated and the ether is washed with cold 50% sulfuric acid, water and sodium bicarbonate; then the ether layer is dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The residue is distilled in vacuo to give 4-pivaloylphenyl acetonitrile (b.p. 143°-148°C/0.75 mm n22 =1.5244.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03962342 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-13536c7b300b43629ac64e1ccf95e851 |
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| Source note | uspto-grants-1976_06 |
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