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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54265Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/54265

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt3-Methyl-2-butenalHCID 61020—
EduktHCID 178478191HCID 178478191—
Katalysatorcopper(I) bromideHCID 24593—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(4-Chlorophenyl)-3-methylbutyraldehydeHCID 1533256638,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622954
Quelldatensatzuspto-grants-1997_04
ORD IDord-9c9e56189438421baff4ea399f4c1945
Quellennotizuspto-grants-1997_04