HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 4-(phenyl-2-thienylmethoxy)-1-[4-(2-nitrophenoxy)-2(E)-butenyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Phenyl-2-thienylmethyl chloride | HCID 10512583 | — |
| Reactant | 4-hydroxy-1-[4-(2-nitrophenoxy)-2(E)-butenyl]piperidine | HCID 19776719 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 4-(phenyl-2-thienylmethoxy)-1-[4-(2-nitrophenoxy)-2(E)-butenyl]piperidine | HCID 19776710 | 65.8% |
Reaction Steps
Into 20 ml of methyl isobutyl ketone were dissolved 2.09 g of phenyl-2-thienylmethyl chloride, 3.50 g of 4-hydroxy-1-[4-(2-nitrophenoxy)-2(E)-butenyl]piperidine and 1.94 g of N,N-diisopropylethylamine, and the resultant solution was heated under reflux with stirring for 2 hours. After cooling, the reaction solution was washed with water, and the solvent was removed under reduced pressure. The residue was eluted with ethanol-chloroform (1:50) by silica gel column chromatography to give 3.06 g of oily 4-(phenyl-2-thienylmethoxy)-1-[4-(2-nitrophenoxy)-2(E)-butenyl]piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190959 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-b8355699bb7b40c680a8e16e51f6c62b |
| Source note | uspto-grants-1993_03 |