関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Cyanide | HCID 9032 | — |
| 反応物 | 1-(2',4'-Difluoro(1,1'-biphenyl)-4-yl)ethan-1-one | HCID 104542 | — |
| 反応物 | 4-Bromoacetyl-2',4'-difluorobiphenyl | HCID 14837387 | — |
| 生成物 | 4-Cyanoacetyl-2',4'-difluorobiphenyl | HCID 21322542 | — |
反応手順
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-bromoacetyl-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°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04151302 |
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| 出典データセット | uspto-grants-1979_04 |
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| ORD ID | ord-eb81bfb4aa45437893a0ff21d116ce4f |
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| 出典メモ | uspto-grants-1979_04 |
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