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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449062Generated: October 31, 2026

1-(2,2-Diphenylethyl)piperidin-4-one → 1-(2,2-Diphenylethyl)-4-methyl-4-piperidinol

https://huagongshe.com/reaction/1449062

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,2-Diphenylethyl)piperidin-4-oneHCID 12515635—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(2,2-Diphenylethyl)-4-methyl-4-piperidinolHCID 20375053—

Reaction Steps

To a stirred solution of 0.28 parts of 1-(2,2-diphenylethyl)-4-piperidinone in 5 parts by volume of tetrahydrofuran under nitrogen atmosphere is added 2 parts by volume of 3 M solution of methylmagnesium bromide. The resultant mixture is stirred for about 2.5 hours and then quenched with the careful addition of 5 parts by volume of 10% ammonium chloride. The mixture is left standing overnight, partitioned between water and ethyl acetate, and the organic layer separated. The organic layer is then dried with brine and magnesium sulfate, and concentrated to give 4-methyl-1-(2,2-diphenylethyl)-4-piperidinol, as yellow solid. This compound is represented by the following structural formula ##STR40##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04188485
Source datasetuspto-grants-1980_02
ORD IDord-147ef1ad2cd4409f887076df6e895135
Source noteuspto-grants-1980_02