Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249159Generated: October 29, 2026

Diisopropylethylamine → Indole

https://huagongshe.com/reaction/249159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBis(4-isobutylphenyl)chloromethaneHCID 19010817—
Reactant3-(3-Aminobenzoyl)indoleHCID 19024726—
SolventDimethylformamideHCID 6228—
ProductIndoleHCID 798210.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212320
Source datasetuspto-grants-1993_05
ORD IDord-99801fe2c9884714a43dcda710968b72
Source noteuspto-grants-1993_05