HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-(3-Hexyl-6-propyl-3-azabicyclo[3.1.0]hex-6-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | 3-Hexyl-6-(3-nitrophenyl)-6-propyl-3-azabicyclo[3.1.0]hexane | HCID 22141282 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(3-Hexyl-6-propyl-3-azabicyclo[3.1.0]hex-6-yl)aniline | HCID 22141308 | 100.3% |
Reaction Steps
To a stirred suspension of 3-hexyl-6-(3-nitrophenyl)-6-propyl-3-azabicyclo[3.1.0]hexane (Preparation 65, 2.60 g, 7.2 mmol), ethanol (150 ml) and iron powder (0.41 g, 73.2 mmol) was added calcium chloride (1.5 g 13.0 nrmnol) in water (50 ml). The reaction mixture was heated under reflux for 16 h. The reaction mixture was cooled to room temperature, filtered through a pad of Celite®, and the mother liquors were concentrated in vacuo. The residue was dissolved in dichloromethane and filtered through a pad of sodium sulphate to give upon concentration the title compound as a yellow oil (2.17 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313312B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-3ad61ebffaba4eb49c8b446b1dfa7cbc |
| Source note | uspto-grants-2001_11 |