Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 5-benzyl-5-(4-bromophenyl)-5H-imidazo[2,1-a]isoindole | HCID 46206599 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58415471 | HCID 58415471 | — |
Reaction Steps
A suspension of 5-benzyl-5-(4-bromophenyl)-5H-imidazo[2,1-a]isoindole (100 mg) in THF (3 mL) was cooled to −78° C. and n-BuLi solution (0.234 mL, 1.6 M in hexane) was added slowly. After stirring for 10 minutes acetone (29 mg) was added to the resulting red solution. After 30 min of the addition of acetone, reaction was quenched with aqueous saturated NH4Cl. The reaction mixture was partitioned between saturated aqueous NH4Cl and EtOAc.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08541595B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-b124a95cab3e49e289e30ce845b760a1 |
|---|
| Source note | uspto-grants-2013_09 |
|---|