HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1439053Erstellt: 27. Oktober 2026
Potassium Cyanide → 4-Cyanoacetyl-2',4'-difluorobiphenyl
https://huagongshe.com/reaction/1439053
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Cyanide | HCID 9032 | — |
| Edukt | 1-(2',4'-Difluoro(1,1'-biphenyl)-4-yl)ethan-1-one | HCID 104542 | — |
| Edukt | Bromacetyl-2',4'-difluorobiphenyl | HCID 21399995 | — |
| Produkt | 4-Cyanoacetyl-2',4'-difluorobiphenyl | HCID 21322542 | — |
Reaktionsschritte
Grignard reagent obtained from 14.2 g. of methyl iodide and 2.4 g. of magnesium in 100 ml. of THF is added dropwise to a solution of 30.4 g. of 3-(2',4'-difluoro-4-biphenylyl)-3-oxopropionic acid ethyl ester, obtained by brominating 4-acetyl-2',4'-difluorobiphenyl to 4 bromacetyl-2',4'-difluorobiphenyl, reacting this with KCN to give 4-cyanoacetyl-2',4'-difluorobiphenyl, hydrolyzing the latter and esterifying the reaction product, in 200 ml. of THF. When the addition is complete, the mixture is heated and stirred for 2 hours more on a water bath and cooled. The resulting alcoholate is hydrolyzed with ice and saturated NH4Cl solution. The ether phase is dried and evaporated to give 3-(2',4'-difluoro-4-biphenylyl)-3-hydroxybutyric acid ethyl ester, m.p. 96°-97°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04057647 |
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| Quelldatensatz | uspto-grants-1977_11 |
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| ORD ID | ord-e15162ec2f664919b634fc05bdb867e9 |
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| Quellennotiz | uspto-grants-1977_11 |
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