HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 70577630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | 3-Benzyl-6-oxa-3-azabicyclo(3.1.0)hexane | HCID 9815370 | — |
| Catalyst | Water | HCID 962 | — |
| Product | HCID 70577630 | HCID 70577630 | — |
Reaction Steps
A mixture of 8.8 g. (0.05 mole) of 1-benzyl-3,4-epoxypyrrolidine, 6.0 g. (0.055 mole) of thiophenol, and 3 drops of water was heated on a steam bath overnight. Upon cooling the mixture, a solid crystallized. The solid was dissolved in methylene chloride and the methylene chloride solution was washed with two 50-ml portions of 5% sodium hydroxide. The methylene chloride layer was dried over anhydrous sodium sulfate and concentrated to give a yellow oil which solidified on standing. The solid was recrystallized from cyclohexane to give 8.6 g. (60%) of a tan solid, m.p. 97°-99°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251541 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-8b3209f6e18046819d951319c4dd9b9e |
| Source note | uspto-grants-1981_02 |