HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aziridine → HCID 86706739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aziridine | HCID 9033 | — |
| Reactant | 1-Methylcyclohexene | HCID 11574 | — |
| Reactant | 1-Decene | HCID 13381 | — |
| Reactant | 1-Azido-4-methylbenzene | HCID 137430 | — |
| Reactant | HCID 86706738 | HCID 86706738 | — |
| Product | HCID 86706739 | HCID 86706739 | — |
Reaction Steps
Selected control reactions following the method of the General Catalytic Reaction were attempted but without [(Me,EtTCPh)Fe(NCCH3)2](PF6)2. These reactions either gave lower yields for aziridines or almost no isolable aziridine. Two example cases are shown. 2-octyl-1-(ptolyl)aziridine. p-Tolyl azide (0.096 g, 0.72 mmol) and 1-decene (1.853 g, 13.2 mmol) were used in the General Catalytic Reaction described above yielding 0.078 g, 43% yield. 1-methyl-7-(p-tolyl)-7-azabicyclo[4.1.0]heptane. p-Tolyl azide (0.203 g, 1.53 mmol) and 1-methylcyclohexene (4.055 g, 42.2 mol) were used in the General Catalytic Reaction described above yielding 0.007 g, 2% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09050589B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-17c4eac939194278a5143ff1429c6480 |
| Source note | uspto-grants-2015_06 |