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HRID 1779409作成日:2026年10月26日

Water → 5-(2-Trifluoromethylphenyl)-4-pentynenitrile

https://huagongshe.com/reaction/1779409

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物Benzene, 1-iodo-2-(trifluoromethyl)-HCID 67957—
反応物4-Cyano-1-butyneHCID 140560—
触媒Copper iodideHCID 83717—
溶媒AcetonitrileHCID 6342—
生成物5-(2-Trifluoromethylphenyl)-4-pentynenitrileHCID 1995553892.9%

反応手順

Under a nitrogen atmosphere, a solution of 15.0 grams (0.055 mole) of 2-trifluoromethylphenyl iodide, 4.8 grams (0.061 mole) of 4-pentynenitrile, 30.6 mL (0.22 mole) of triethylamine, 0.4 gram (0.0006 mole) of bis(triphenylphosphine)palladium(11) chloride, and 0.1 gram (0.0006 mole) of copper(11) iodide in 50 mL of acetonitrile was stirred at ambient temperature for 5 hours. After this time, gas chromatographic analysis (GC) of the reaction mixture indicated that the reaction was about 60% complete. The reaction mixture was warmed to 40°-45° C., where it was stirred for 16 hours. After this time the reaction mixture was poured into 300 mL of water, and the mixture was extracted with two 100 mL portions of diethyl ether. The combined extracts were washed with aqueous dilute hydrochloric acid and then were dried with magnesium sulfate. The mixture was filtered and concentrated under reduced pressure to a residual oil. The oil was subjected to column chromatography on silica gel. Elution was accomplished using 1:1 - methylene chloride and petroleum ether. The product-containing fractions were combined and concentrated under reduced pressure, yielding 11.4 grams of 5-(2-trifluoromethylphenyl)-4-pentynenitrile. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05627189
出典データセットuspto-grants-1997_05
ORD IDord-dbd975ee96c041e49c85343f740c2ccb
出典メモuspto-grants-1997_05