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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413699Generated: October 30, 2026

Ammonia → HCID 20290315, compound

https://huagongshe.com/reaction/1413699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantChlorocyclohexaneHCID 10952—
Reactant2-Cyclopenten-1-oneHCID 13588—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantCyclopentanone, 3-cyclohexyl-HCID 11105726—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20290315HCID 2029031560%

Reaction Steps

3-Cyclohexyl-cyclopentanone used hereinabove as starting material was prepared as indicated hereinafter: 16.6 g (0.148 Mole) of cyclohexyl chloride were added dropwise to 3.6 g (0.150 atome-g) of magnesium metal in a 250 ml vessel, under nitrogen atmosphere and in the presence of a iodine cristal. The reaction mixture was heated to reflux for 1 hour, then cooled to 0° and 1.42 g (0.074 Mole) of cuprous iodide were added thereto. After cooling the reaction mixture at -8°, 5.74 g (0.070 Mole) of cyclopent-2-ene-1-one in 40 ml of tetrahydrofurane were added dropwise. After having been stirred for 1 hour at -8°, the reaction mixture was poured onto 100 g of crushed ice, acidified with 15% HCl in water (pH 4-5) and finally neutralized by the addition of aqueous ammonia. After the addition of 10 g of NH4Cl the reaction mixture was extracted with ether (3×300 ml), washed with water (3×100 ml), dried over sodium sulfate and finally evaporated to afford 13.2 g of raw material. After purification by means of column chromatography (neutral Al2O3 --eluent:toluene) and subsequent distillation on a VIGREUX column, there were obtained 7.0 g (60% yield) of the desired product, b.p. 50°/0.005 Torr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251398
Source datasetuspto-grants-1981_02
ORD IDord-52b76aefbe504e29bea110c623960527
Source noteuspto-grants-1981_02