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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166611Generated: November 1, 2026

Ammonium Chloride → 1-(1-Phenylcyclopropyl)ethan-1-one

https://huagongshe.com/reaction/1166611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 18000813HCID 18000813—
ReactantHCID 178418348HCID 178418348—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Phenylcyclopropyl)ethan-1-oneHCID 12257263—

Reaction Conditions

Temperature-10 °C

Reaction Steps

4.34 g of 27 is dissolved in 189 ml of THF, cooled to −10° C., and 21.5 ml of methyllithium solution (1.6 M in diethyl ether) is added in drops under nitrogen. It is stirred for 2 hours at this temperature, and the reaction mixture is then poured into saturated ammonium chloride solution. After extraction with ethyl acetate, the organic phase is dried on sodium sulfate and concentrated by evaporation. The residue is chromatographed on silica gel with ethyl acetate/hexane, whereby 3.7 g of title compound 28 is obtained as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613920B1
Source datasetuspto-grants-2003_09
ORD IDord-0ab13ffa5f604d4db40a866c0f150629
Source noteuspto-grants-2003_09