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HRID 54256作成日:2026年10月23日

Ammonium Chloride → 3-(4-Fluorophenyl)-3-methylbutyraldehyde

https://huagongshe.com/ja/reaction/54256

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物3-Methyl-2-butenalHCID 61020—
反応物HCID 178418676HCID 178418676—
触媒copper(I) bromideHCID 24593—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-Fluorophenyl)-3-methylbutyraldehydeHCID 2146801243%

反応条件

温度5 °C

反応手順

Under a nitrogen atmosphere, a stirring solution of 66.6 grams (0.334 mole) of 4-fluorophenylmagnesium bromide (1M in diethyl ether) is cooled to -10° C., and 2.2 grams (0.015 mole) of copper(I) bromide is added in one portion. Upon completion of addition, a solution of 25.0 grams (0.297 mole) of 3-methyl-2-butenal in 20 mL of tetrahydrofuran is added dropwise at a rate to maintain the reaction mixture temperature at about 5° C. The complete addition requires about one hour. Upon completion of addition, the reaction mixture is stirred for one additional hour and then is stored in a refrigerator for about 18 hours. After this time the reaction mixture is poured into 500 mL of aqueous ammonium chloride and extracted with four portions of diethyl ether. The combined extracts are concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel, using methylene chloride as the eluant. The product-containing fractions are combined and concentrated under reduced pressure to a residue. The residue is subjected to a second column chromatography on silica gel, using 100% petroleum ether and combinations of methylene chloride in petroleum ether. The product-containing fractions are combined and concentrated under reduced pressure, yielding about 23.0 grams of 3-(4-fluorophenyl)-3-methylbutyraldehyde. The NMR spectrum is consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622954
出典データセットuspto-grants-1997_04
ORD IDord-74247e5a08c9439fb977ff6250e38b1e
出典メモuspto-grants-1997_04