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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566688Generated: October 31, 2026

Benzyl Bromide → 1h-Indole,2-ethyl-4-nitro-1-(phenylmethyl)-

https://huagongshe.com/reaction/566688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
Reactant2-ethyl-4-nitro-1H-indoleHCID 13047994—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1h-Indole,2-ethyl-4-nitro-1-(phenylmethyl)-HCID 1054071091%

Reaction Steps

2-Ethyl-4-nitro-1H-indole (4.75 g, 25 mmol) was added to a mixture of 1.0 g (25 mmol) of 60% NaH/mineral oil (washed with hexane before adding DMF) in 40 ml DMF. After 45 minutes, 3.0 ml (25 mmol) of benzyl bromide was added. The mixture was stirred at room temperature for four hours, diluted with water, and extracted with EtOAc. The EtOAc solution was washed with brine, dried over MgSO4, and evaporated in vacuo. The residue was chromatographed on silica gel eluting with 20% EtOAc/Hexane to give 6.36 g (91%) of 1-Phenylmethyl-2-ethyl-4-nitro-1H-indole as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06175021B1
Source datasetuspto-grants-2001_01
ORD IDord-d3da996996374ebb8cae2ccd9ce03060
Source noteuspto-grants-2001_01