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HRID 54265作成日:2026年10月26日

Water → 3-(4-Chlorophenyl)-3-methylbutyraldehyde

https://huagongshe.com/reaction/54265

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-Methyl-2-butenalHCID 61020—
反応物HCID 178478191HCID 178478191—
触媒copper(I) bromideHCID 24593—
溶媒TetrahydrofuranHCID 8028—
生成物3-(4-Chlorophenyl)-3-methylbutyraldehydeHCID 1533256638.6%

反応手順

Under a nitrogen atmosphere, a stirred solution of 21.6 grams (0.10 mole) of 4-chlorophenylmagnesium bromide (1M in diethyl ether) in 100 mL of tetrahydrofuran is cooled to -15° C., and 0.7 grams (catalyst) of copper(I) bromide is added in one portion. Upon completion of addition, 9.7 mL (0.10 mole) of 3-methyl-2-butenal is added dropwise during a 1.5 hour period, while maintaining the reaction mixture temperature below -10° C. Upon completion of addition, the reaction mixture is allowed to warm to ambient temperature, where it is stirred for about 18 hours. The reaction mixture is then poured into 300 mL of water and extracted with two 200 mL portions of diethyl ether. The combined extracts are dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure to a residue. The residue is subjected to column chromatography on silica gel, using 50% petroleum ether in methylene chloride as the eluant. The appropriate product-containing fractions are combined and concentrated under reduced pressure, yielding 7.6 grams of 3-(4-chlorophenyl)-3-methylbutyraldehyde. The NMR spectrum is consistent with the proposed structure. The reaction is repeated.

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-9c9e56189438421baff4ea399f4c1945
出典メモuspto-grants-1997_04