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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394432Generated: October 29, 2026

Indole-3-Carboxaldehyde → HCID 6422043, compound

https://huagongshe.com/reaction/2394432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-CarboxaldehydeHCID 10256—
Reactant(1-Bromoethyl)benzeneHCID 11454—
ProductHCID 6422043HCID 6422043—

Reaction Steps

The same procedures used in Example 1 were repeated except for using 870 mg of indole-3-carbaldehyde and α-phenylethyl bromide in place of the benzyl bromide used in Example 1 to give 1.42 g of 1-(α-methylbenzyl)indole-3-carbaldehyde as an orange-colored oily substance. The yield thereof was found to be 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811439
Source datasetuspto-grants-1998_09
ORD IDord-458b81be13a94f68848d2c2ad1553ad3
Source noteuspto-grants-1998_09