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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349356Generated: October 31, 2026

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

https://huagongshe.com/reaction/1349356

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 numberUS07211680B2
Source datasetuspto-grants-2007_05
ORD IDord-f3c2d8351f5f48d4a34b006c12ff17d6
Source noteuspto-grants-2007_05