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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37978Generated: October 25, 2026

Water → 1-benzyl-1H-indol-3-ylacetonitrile

https://huagongshe.com/reaction/37978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
ReactantIndole-3-acetonitrileHCID 351795—
SolventMethanolHCID 887—
Product1-benzyl-1H-indol-3-ylacetonitrileHCID 11032169—

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 3-indolylacetonitrile (5 g, 32 mmol), triton B (40% in MeOH, 0.5 g), benzyl bromide (7. 8 mL, 2 eq.) and aqueous NaOH (50%, 12.6 mL) was stirred for 2 hours at 20° C. Water was added. Solid was collected by filtration and washed with water and hexane and dried under high vacuum to give [1-benzyl-1H-indol-3-yl]acetonitrile (6.97 g). MS (ES): 247 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524704B2
Source datasetuspto-grants-2013_09
ORD IDord-08afda3e79734efdb85638397638806e
Source noteuspto-grants-2013_09