HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → Indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Bis(4-isobutylphenyl)chloromethane | HCID 19010817 | — |
| Reactant | 3-(3-Aminobenzoyl)indole | HCID 19024726 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Indole | HCID 798 | 210.1% |
Reaction Steps
To a solution of 3-(3-aminobenzoyl)indole (1.2 g) in N,N-dimethylformamide (12 ml) were added diisopropylethylamine (1.77 ml) and a solution of bis(4-isobutylphenyl)chloromethane (1.92 g) in N,N-dimethylformamide (5 ml) at 25° C., and the mixture was allowed to stand at the same temperature for 14 hours. The reaction mixture was partitioned between ethyl acetate and water, and the organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel (50 g) eluting with a mixture of ethyl acetate and chloroform (1:20) to give 3-[3-bis(4-isobutylphenyl)methylamino]benzoyl]indole (1.25 g) as pale yellow amorphous powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05212320 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-99801fe2c9884714a43dcda710968b72 |
| Source note | uspto-grants-1993_05 |