HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromodiphenylmethane → 4-Diphenylmethoxy1-[3-methyl-3-(2-nitrophenoxy)propyl]piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | 4-Hydroxy-1-[3-methyl-3-(2-nitrophenoxy)propyl]piperidine | HCID 19776715 | — |
| Reactant | 4-Hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidine | HCID 19776793 | — |
| Product | 4-Diphenylmethoxy1-[3-methyl-3-(2-nitrophenoxy)propyl]piperidine | HCID 19776785 | — |
Reaction Steps
The procedure of Example 1 (a) was repeated except for using diphenylmethyl bromide and 4-hydroxy-1-[3-methyl-3-(2-nitrophenoxy)propyl]piperidine instead of diphenylmethyl bromide and 4-hydroxy-1-[3-(2-nitrophenoxy)propyl]piperidine to give oily 4-diphenylmethoxy1-[3-methyl-3-(2-nitrophenoxy)propyl]piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190959 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-ab635ec9eb2641ea9e1a16ad5c91cb5d |
| Source note | uspto-grants-1993_03 |