Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762482Generated: October 31, 2026

Benzaldehyde → HCID 20041368, compound

https://huagongshe.com/reaction/1762482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant5-CyanotryptamineHCID 58926—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHCID 20041368HCID 2004136851.1%

Reaction Steps

Freshly distilled benzaldehyde (2.96 g) was added to a solution of 3-(2-aminoethyl)-1H-indole-5-carbonitrile (5 g) in absolute ethanol (120 ml). The mixture was heated at reflux for 2 h before cooling to 10°. Sodium borohydride (1 g) was added and the suspension stirred for 2 h. The mixture was reduced to dryness and the residue recrystallised from a mixture of toluene and petroleum ether (b.p. 60°-80°). The solid was washed well with water and dried to give the title compound as a powder (3.8 g), m.p 99°-101°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04833153
Source datasetuspto-grants-1989_05
ORD IDord-4421b81fe0ac46beb4d752b49596856b
Source noteuspto-grants-1989_05