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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112289Generated: October 25, 2026

Ethanol → HCID 12822305, compound

https://huagongshe.com/reaction/1112289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
Reactant1-Cyclohexyl-4-chloromethyl-3,3-diphenyl-2-pyrrolidinoneHCID 12822293—
SolventMethanolHCID 887—
SolventChloroform methanolHCID 21584188—
ProductHCID 12822305HCID 12822305—

Reaction Steps

A mixture of 39 g. (0.106 mole) of 4-chloromethyl-1-cyclohexyl-3,3-diphenyl-2-pyrrolidinone, 58.5 g. (0.424 mole) of finely ground potassium carbonate, and 22.5 g. (0.106 mole) of 4-(4-chlorophenyl)-4-hydroxypiperidine in 300 ml. of ethanol was heated to 200° C. in a steel bomb for 66 hrs. During the heating the bomb was continuously rotated to produce mild stirring. The contents were filtered and the filtrate concentrated. The residue was heated in 250 ml. of ethylacetate and allowed to stand at room temperature overnight. The mixture was filtered. The filtrate was extracted with dilute hydrochloric acid and dilute sodium hydroxide. The ethylacetate was concentrated and the residue dissolved in ethanol and allowed to stand overnight. The resulting mixture was filtered and the filtrate concentrated. The residue was chromatographed on a 4.5 × 60 cm. silica gel column. The product was obtained from the column using a chloroform-methanol eluate containing increasing amounts of methanol. The product after isolation and crystallization from isopropanol melted at 222°-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04120969
Source datasetuspto-grants-1978_10
ORD IDord-4616da6b6c0b4ec5a999e703401ab0ea
Source noteuspto-grants-1978_10