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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742331Generated: November 1, 2026

5-Nitroindole → HCID 86748077, compound

https://huagongshe.com/reaction/1742331

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NitroindoleHCID 22523—
Reactant4-(Bromomethyl)-3-methoxybenzonitrileHCID 14752995—
CatalystSilver(II) oxideHCID 92152—
CatalystHCID 178418778HCID 178418778—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86748077HCID 8674807730.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

An efficiently stirred mixture of 5-nitroindole (3.24 g.), bromide (W) (4.57 g.) and silver (I) oxide (4.87 g.) in dry dioxane (90 ml.) was heated at 100° C. for 5 hours. Additional silver oxide (2 g.) was added, and heating continued for 1 hour. The cooled mixture was evaporated, the residue diluted with dichloromethane, filtered, washing the filter cake with dichloromethane until the washings were colorless, and the combined filtrate evaporated. The product was purified by flash chromatography on silica gel, eluting with 3:7 v/v ethyl acetate:hexane, giving a product which was crystallized from a mixture of ethyl acetate and hexane to give 3-(4-cyano-2-methoxybenzyl-5-nitroindole (1.87 g., 30% ) as a yellow powder, m.p. 204°-206° C.; partial NMR (80 MHz, DMSO--d6): 3.92(s,3H, OMe); 4.12(s,2H, ArCH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338734
Source datasetuspto-grants-1994_08
ORD IDord-3cb15abeaef9479dbe92ef7025d4ae37
Source noteuspto-grants-1994_08