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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394435Generated: October 29, 2026

Indole-3-Carboxaldehyde → HCID 18973376, compound

https://huagongshe.com/reaction/2394435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-CarboxaldehydeHCID 10256—
ReactantHCID 18973573HCID 18973573—
ProductHCID 18973376HCID 18973376—

Reaction Steps

The same procedures used in Example 1 were repeated except for using 870 mg of indole-3-carbaldehyde and 2-methoxybenzyl methanesulfonate in place of the benzyl bromide used in Example 1 to give 926 mg of 1-(2-methoxybenzyl)indole-3-carbaldehyde as pale yellow crystals. The yield thereof was found to be 58%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811439
Source datasetuspto-grants-1998_09
ORD IDord-eb76a7e815d94b9ea4136108d6364b51
Source noteuspto-grants-1998_09