Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394444Generated: October 29, 2026

Indole-3-Carboxaldehyde → HCID 18973550, compound

https://huagongshe.com/reaction/2394444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-CarboxaldehydeHCID 10256—
ReactantHCID 18973462HCID 18973462—
ProductHCID 18973550HCID 18973550—

Reaction Steps

The same procedures used in Example 1 were repeated except for using 435 mg of indole-3-carbaldehyde and 4-benzyloxybenzyl methanesulfonate in place of the benzyl bromide used in Example 1 to give 626 mg of 1-(4-benzyloxybenzyl)indole-3-carbaldehyde as colorless crystals. The yield thereof was found to be 61%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811439
Source datasetuspto-grants-1998_09
ORD IDord-603dc0aba62a4232b32214a9cba821cf
Source noteuspto-grants-1998_09