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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902860Generated: November 1, 2026

Tetrahydrofuran → 76825-10-0

https://huagongshe.com/reaction/1902860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(4-Chlorophenyl)-4-(dimethylamino)cyclohexan-1-oneHCID 12595650—
ReactantHCID 178418573HCID 178418573—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product76825-10-0HCID 12711949—

Reaction Steps

To an ice-cooled solution of 10 ml. of 3 M methyl magnesium bromide in Et2O is added a solution of 1.25 g. (0.005 mole) of 4-(p-chlorophenyl)-4-(dimethylamino)cyclohexanone in 25 ml. of tetrahydrofuran. The mixture is stirred under nitrogen in the cold for one-half hour and then at room temperature for forty-eight hours. Following ice bath cooling there is added 20 ml. of saturated aqueous ammonium chloride, 10 ml. of water, 10 ml. diethyl ether and 25 ml. benzene. The organic layer is washed with 10 ml. water and 10 ml. brine and taken to dryness. The residue is chromatographed on a 1"×48" high pressure liquid chromatography column (elution with 3% MeOH in chloroform). Starting ketone is first eluted followed by a second material. Those fractions containing the second material are combined, concentrated to dryness and crystallized from CH3CN:H2O to yield 0.20 g. of the tertiary alcohol, melting point 119°-120°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04366172
Source datasetuspto-grants-1982_12
ORD IDord-764e8a050554463090ba1e70748af37e
Source noteuspto-grants-1982_12