HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2,2-Diphenylethyl)piperidin-4-one → 1-(2,2-Diphenylethyl)-4-methyl-4-piperidinol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2,2-Diphenylethyl)piperidin-4-one | HCID 12515635 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2,2-Diphenylethyl)-4-methyl-4-piperidinol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04188485 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-147ef1ad2cd4409f887076df6e895135 |
| Source note | uspto-grants-1980_02 |