HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 12804759, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 12542600 | HCID 12542600 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12804759 | HCID 12804759 | — |
Reaction Steps
2.0 g of 1-methyl-4-(α-phenyl-2-tolyl)-4-piperidinol, Example 1, is treated with 10 ml of benzoyl chloride with stirring and cooling. The reaction solution is diluted with 20 ml of ether, stirred for two hours and the resulting precipitate collected by suction filtration. The filter cake is washed well with ether and dried in vacuo at 40° C. over sodium hydroxide pellets. The dried filter cake is recrystallized twice from a chloroform-ether mixture to give colorless crystals, mp 197°-198° C. of 4-benzoyloxy-1-methyl-4-(α-phenyl-2-tolyl)piperidine hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04311703 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-6b09cb985b304b2ab9159232df113ea7 |
| Source note | uspto-grants-1982_01 |