HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Phenyl-7-oxa-3-azabicyclo[4.1.0]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | 4-Phenyl-1,2,5,6-tetrahydropyridine hydrobromide | HCID 20574114 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Phenyl-7-oxa-3-azabicyclo[4.1.0]heptane | HCID 12929375 | — |
Reaction Steps
A solution of 33.6 g of bromine and 60 g of sodium bromide in 450 ml of water was added dropwise with stirring to solution comprising 50 g of 4-phenyl-1,2,5,6-tetrahydropyridine hydrobromide in 600 ml of water and the reaction mixture was then stirred at room temperature for 30 minutes. The solution was stirred on an ice bath while 252 ml of 10% sodium hydroxide was added dropwise thereto. The resulting mixture then being stirred at room temperature for a further 30 minutes. The aqueous solution was extracted with methylene chloride and the organic phase solution dried over sodium sulfate and then concentrated in vacuo to give 25.2 g of the desired 3,4-epoxy-4-phenyl piperidine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04286095 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-672e5faeeda843dba3654189040b632c |
| Source note | uspto-grants-1981_08 |