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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394440Generated: October 29, 2026

Indole-3-Carboxaldehyde → Oncrasin 1

https://huagongshe.com/reaction/2394440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-3-CarboxaldehydeHCID 10256—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
ProductOncrasin 1HCID 87244592%

Reaction Steps

The same procedures used in Example 1 were repeated except for using 2.98 g of 4-chlorobenzyl bromide and 2.00 g of indole-3-carbaldehyde as a starting material to give 3.42 g of 1-(4-chlorobenzyl)indole-3-carbaldehyde as pale yellow crystals. The yield thereof was found to be 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811439
Source datasetuspto-grants-1998_09
ORD IDord-6775f21ae8924d4c93f01ed5186822d3
Source noteuspto-grants-1998_09