Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Propionate | HCID 7749 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 1-Phenyl-2-butanone | HCID 13879 | 53.3% |
Reaction Steps
In a 2-liter flask provided with a thermometer, stirrer, dropping funnel and reflux condenser 600 ml of absolute alcohol are treated portionwise while stirring with 30 g of sodium metal and the mixture is held at reflux temperature until the metal has dissolved. Within 0.5 hour there is added dropwise to the boiling solution a mixture of 117.2 g of benzyl cyanide and 153.2 g of ethyl propionate and the mixture is heated for a further 3 hours. The alcohol is then distilled off and there are added 300 ml of toluene, followed by 250 ml of ice/water. The aqueous phase is separated, washed with 300 ml of toluene and then 540 g of 96% sulphuric acid are added. The mixture is held at reflux temperature until the evolution of carbon dioxide ceases, cooled, diluted with 250 ml of ice/water and extracted with two 300 ml portions of toluene. The toluene extracts are washed with water, with 10% sodium carbonate solution and again with water, dried over sodium sulphate and evaporated. Distillation gives 79 g of ethyl benzyl ketone of boiling point 69° C./3 mmHg; nD20 =1.5109; yield 53%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04481133 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-883d54c20515486a8b8ddb22480bde97 |
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| Source note | uspto-grants-1984_11 |
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