Potassium Cation → Phenyl-(1-triisopropylsilanyl-1H-indol-4-yl)-amine

HRID 215090Notes

Reaction equation

HRID 215090 reaction equation
[Br:8][c:9]1[c:10]2[cH:11][cH:12][n:13]([Si:18]([CH:19]([CH3:20])[CH3:21])([CH:22]([CH3:23])[CH3:24])[CH:25]([CH3:26])[CH3:27])[c:14]2[cH:15][cH:16][cH:17]1.[C:34]([OH:35])([CH3:36])([CH3:37])[CH3:38].[K+:28].[K+:29].[NH2:1][c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1.[O-:30][C:31]([O-:32])=[O:33]>>[NH:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[c:9]1[c:10]2[cH:11][cH:12][n:13]([Si:18]([CH:19]([CH3:20])[CH3:21])([CH:22]([CH3:23])[CH3:24])[CH:25]([CH3:26])[CH3:27])[c:14]2[cH:15][cH:16][cH:17]1

Participants

6

Reactant 5

HCID 813Potassium Cation2×HCID 6115AnilineHCID 6386tert-ButanolHCID 19660Carbonate IonHCID 27955734-bromo-1-(triisopropylsilyl)-1H-indole

Product 1

HCID 59831613Phenyl-(1-triisopropylsilanyl-1H-indol-4-yl)-amine

Sources & evidence

ORD record
ord-829c505a1bbd4b7498117aa0eb55b876
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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