HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → 1-Propanone, 1-[4-(phenylamino)-1-(2-phenylethyl)-4-piperidinyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 1-Propanone, 1-[4-(phenylamino)-4-piperidinyl]- | HCID 12298227 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Propanone, 1-[4-(phenylamino)-1-(2-phenylethyl)-4-piperidinyl]- | HCID 12298222 | — |
Reaction Steps
A solution of 2.7 parts of (2-bromoethyl)benzene), 3.1 parts of 1-[4-(phenylamino)-4-piperidinyl]-1-propanone and 2.6 parts of N,N-diethylethanamine in 18 parts of N,N-dimethylacetamide is stirred for 4h. 30 at 80° C. The reaction mixture is poured onto 100 parts of water and the product is extracted with benzene. The extract is washed with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The oily residue is crystallized from 2,2'-oxybispropane, yielding 1-[4-(phenylamino)-1-(2-phenylethyl)-4-piperidinyl]-1-propanone; mp. 105.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998834 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-59225f01d7c94b569e9a814b59d69817 |
| Source note | uspto-grants-1976_12 |