HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 3-Hydroxy-1-methyl-4-phenyl-4-phenylthio-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Methyl-6-phenyl-7-oxa-3-azabicyclo[4.1.0]heptane | HCID 435091 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 3-Hydroxy-1-methyl-4-phenyl-4-phenylthio-piperidine | HCID 12929368 | 86.8% |
Reaction Steps
9.6 Ml of 10% sodium hydroxide solution was added to a solution of 2.46 ml (0.024 mole) of thiophenol in 15 ml of ethylene glycol and the resulting solution stirred at room temperature for five minutes. 1.9 G (0.01 mole) of 3,4-epoxy-1-methyl-4-phenyl-piperidine was added with stirring to the above solution and the resulting solution stirred at room temperature for a further one hour. A solid began to separate after five minutes. The solid was filtered and suspended in acetone. Filtration of the solid gave 2.6 g of 3-hydroxy-1-methyl-4-phenyl-4-phenylthio-piperidine as a white solid having a melting point of 217°-9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04286095 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-78db829290b64018a583c854a0d0133c |
| Source note | uspto-grants-1981_08 |