Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 22390429 | HCID 22390429 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 22390462 | HCID 22390462 | — |
Reaction Steps
5.6 ml of a 15% solution of n-butyllithium in hexane are added, at −78° C., to 3.1 g of 1-[3-(4-bromo-3-chlorophenyl)prop-2-ynyl]azepane (compound Ia.7) in 50 ml of diethyl ether and stirring is maintained at −75° C. for 1 hour. Still at −78° C., 1.38 g of 2-amandatanone in 25 ml of diethyl ether are added, and the reaction mixture is then stirred for 1 hour at −78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06908914B1 |
|---|
| Source dataset | uspto-grants-2005_06 |
|---|
| ORD ID | ord-5688f36b5f244cf4a56eac1660b4d96e |
|---|
| Source note | uspto-grants-2005_06 |
|---|