HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111063Generated: October 31, 2026
Hydrochloric Acid → Ethyl 3-cyano-2-phenylpropanoate
https://huagongshe.com/reaction/1111063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl phenylacetate | HCID 7590 | — |
| Reactant | Iodoacetonitrile | HCID 69356 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-cyano-2-phenylpropanoate | HCID 15672492 | 86.4% |
Reaction Steps
In this example 10 g of ethyl phenylacetate in 10 ml of THF was added dropwise to 61 ml of a 1 molar solution lithium bis[trimethylsilvllamide in tetrahydrofuran, under nitrogen, at -78° C. The mixture was stirred for one hour at -78° C. A solution containing 10.2 g of iodoacetonitrile in 10 ml of tetrahydrofuran was added dropwise. The reaction mixture was stirred at -78° C. for about one-half hour and then stirred for two hours and allowed to warm toward room temperature during this period. The reaction mixture was then added to water and the pH adjusted to pH 1 by the addition of aqueous 10% hydrochloric acid. The mixture was washed with saturated aqueous sodium chloride solution and extracted three times with ethyl ether. The extracts were combined, washed twice with aqueous saturated sodium bicarbonate, dried over magnesium sulfate and evaporated affording 10.7 g of the title compound is an oil. The oil was further purified by chromatography over silica gel eluting with 20% vol. ethyl acetate petroleum ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04978386 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-3c2a651d079444a298bc643e9b9cfc87 |
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| Source note | uspto-grants-1990_12 |
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