関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ether, ethyl ethynyl | HCID 61239 | — |
| 反応物 | 1-(2',4'-Difluoro(1,1'-biphenyl)-4-yl)ethan-1-one | HCID 104542 | — |
| 反応物 | HCID 178418443 | HCID 178418443 | — |
| 反応物 | HCID 178467907 | HCID 178467907 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(2',4'-Difluoro-4-biphenylyl)-2-butenoic acid ethyl ester | HCID 54108058 | — |
反応手順
A solution of 23.2 g. of 4-acetyl-2',4'-difluorobiphenyl in 50 ml. of THF and 50 ml. of ether is added slowly dropwise to a solution of 17.5 g. of ethoxyethinylmagnesium bromide in 200 ml. of ether, prepared by reacting ethoxyacetylene with ethyl magnesium bromide. The mixture is stirred for 1 hour at 20°. The reaction product is hydrolyzed with ice water/ammonium chloride and extracted with ether. The combined ether extracts are dried over MgSO4 and evaporated. Residual 1-ethoxy-3-(2',4'-difluoro-4-biphenylyl)-butyn-3-ol is dissolved in 200 ml. of 95% ethanol and 0.05 g. of solid CO2 is added to the solution and the mixture is left to stand for 12 hours at 20°. The customary work up gives 3-(2',4'-difluoro-4-biphenylyl)-2-butenoic acid ethyl ester, m.p. 54°-56°.
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-efe2eda672c94945a3f99d096be0d5a2 |
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| 出典メモ | uspto-grants-1979_04 |
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