Indole-3-Carboxaldehyde → HCID 18973487, compound

HRID 2394436Notes

Reaction equation

HRID 2394436 reaction equation
Br[CH2:2][CH2:3][CH:4]=[C:5]([CH3:7])[CH3:6].[NH:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([CH:17]=[O:18])=[CH:9]1>>[CH3:6][C:5]([CH3:7])=[CH:4][CH2:3][CH2:2][N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([CH:17]=[O:18])=[CH:9]1

Participants

3

Reactant 2

HCID 10256Indole-3-CarboxaldehydeHCID 1375215-Bromo-2-methyl-2-pentene

Product 1

HCID 18973487HCID 18973487, compoundYield 97.7%

Procedure

The same procedures used in Example 1 were repeated except for using 2.52 g of 5-bromo-2-methyl-2-pentene and 2.00 g of indole-3-carbaldehyde as a starting material to give 3.06 g of 1-(4-methyl-3-pentenyl)indole-3-carbaldehyde as colorless crystals. The yield thereof was found to be 98%.

Sources & evidence

ORD record
ord-4b05ef32be374113af970dd67d023541
Source dataset
uspto-grants-1998_09
Patent number
US05811439

Reaction notes

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