Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847163Generated: November 1, 2026

p-Bromochlorobenzene → 1-Methycyclopropyl 4-chlorophenyl ketone

https://huagongshe.com/reaction/847163

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromochlorobenzeneHCID 7806—
ReactantEthyl AcetateHCID 8857—
ReactantN,1-Dimethoxy-N-methylcyclopropane-1-carboxamideHCID 19882457—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-Methycyclopropyl 4-chlorophenyl ketoneHCID 6789540097%

Reaction Conditions

Temperature0 °C

Reaction Steps

22 ml (0.036 mol) of a 1.6 molar n-butyl-lithium solution are added at -78° C. with stirring to a mixture of 6.9 g (0.036 mol) of 4-bromochlorobenzene and 70 ml of diethyl ether. The reaction mixture is warmed to 0° C. and stirred at this temperature for 15 minutes. After cooling to -78° C. again, a solution of 4.8 g (0.03 mol) of N-methoxy-N-methyl-1-methoxycyclopropane-carboxamide in 20 ml of diethyl ether is added rapidly. The mixture is then subsequently stirred at -78° C., at 0° C. and at room temperature, in each case for one hour. 20 ml of ethyl acetate are then added to the reaction mixture, which is stirred for 5 minutes and then poured into ice-water. The resulting mixture is extracted three times with ethyl acetate, and the combined organic phases are dried over sodium sulphate and then concentrated by stripping off the solvent under reduced pressure. 6.1 g (97% of theory) of 1-methycyclopropyl 4-chlorophenyl ketone are obtained in this manner and are reacted further without prior purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140035
Source datasetuspto-grants-1992_08
ORD IDord-b0a4f4e81c824cebbda9ae918154be97
Source noteuspto-grants-1992_08