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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448558Generated: November 1, 2026

Acetone → 4-Methylamino-4-phenylcyclohexanone hydrochloride

https://huagongshe.com/reaction/1448558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methylamino-4-phenylcyclohexanoneHCID 13345270—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product4-Methylamino-4-phenylcyclohexanone hydrochlorideHCID 2045334774%

Reaction Steps

A reaction mixture consisting of 1.0 gm. (0.0035 mole) of 4-methylamino-4-phenylcyclohexanone, ethylene ketal, hydrochloride (prepared in Example 17, Part G, above) 2.0 ml. of 2.5 N hydrochloric acid, and 20 ml. acetone is stirred continuously for eighteen (18) hours, at 25° C. The reaction mixture is then made basic by adding solid sodium bicarbonate, and most of the solvent is removed by evaporation under reduced pressure. The concentrated material thus obtained is ectracted four times with 20 ml. portions of methylene chloride. The extracts are combined and the methylene chloride is removed by evaporation under reduced pressure. A gummy residue is obtained that is dissolved in diethyl ether. The ether solution is treated with hydrogen chloride in ether. A precipitate forms which is collected on a filter and recrystallized from a mixture of methylene chloride and ethyl acetate. There is thus obtained 0.53 gm. (74% yield) of 4-methylamino-4-phenylcyclohexanone hydrochloride having a melting range from 218° to 220° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04180584
Source datasetuspto-grants-1979_12
ORD IDord-40429186790b4ac89245533e19ed41a4
Source noteuspto-grants-1979_12