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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394408Generated: November 1, 2026

Indole-4-carboxaldehyde → HCID 18973428, compound

https://huagongshe.com/reaction/2394408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-4-carboxaldehydeHCID 333703—
ReactantHCID 18973501HCID 18973501—
ProductHCID 18973428HCID 18973428—

Reaction Steps

The same procedures used in Example 1 were repeated except for using 725 mg of indole-4-carbaldehyde and 2-trifluoromethylbenzyl methanesulfonate in place of the benzyl bromide used in Example 1 to give 1.44 g of 1-(2 -trifluoromethylbenzyl)indole-4-carbaldehyde as a yellow 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-a953bd2ed3174c8baa93267eee48e68c
Source noteuspto-grants-1998_09