HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-[2-(3-Bromophenyl)propyl]-2-(cyclohexylmethyl)piperidine | HCID 12805099 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | Acetophenone | HCID 7410 | — |
Reaction Steps
Following a procedure similar to that described in Example 3, 37.8 g. (0.1 mole) of 2-cyclohexylmethyl-1-[2-(3-bromophenyl)propyl]piperidine was reacted with 0.18 mole of n-butyl lithium in diethyl ether and the resulting lithio derivative reacted directly with 27 g. (0.23 mole) of acetophenone to give 11.8 g. of 2-cyclohexylmethyl-1-{2-[3-(α-hydroxy-α-methylbenzyl)phenyl]propyl}piperidine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04216326 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-d028c6b173f24b03b03072544847300e |
| Source note | uspto-grants-1980_08 |