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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939686Generated: October 30, 2026

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

https://huagongshe.com/reaction/1939686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Methyl-2-butenalHCID 61020—
ReactantHCID 178478191HCID 178478191—
Catalystcopper(I) bromideHCID 24593—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Chlorophenyl)-3-methylbutyraldehydeHCID 1533256638.6%

Reaction Steps

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696259
Source datasetuspto-grants-1997_12
ORD IDord-49497d1423a740e9be883aa34c088182
Source noteuspto-grants-1997_12