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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56237Generated: October 26, 2026

Diiodomethane → 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile

https://huagongshe.com/reaction/56237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
Reactant3-CyanophenolHCID 13394—
ReactantSodium hydrideHCID 24758—
Reactant6-Nitro-1H-indoleHCID 78502—
SolventDimethylformamideHCID 6228—
Product3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrileHCID 9003044751%

Reaction Steps

To a mixture of NaH (3.0 g, 75.0 mmol, 60%) in DMF (20 mL) were added a solution of 6-nitro-1H-indole (4.86 g, 30.0 mmol) in DMF (10 mL) and a solution of 3-hydroxybenzonitrile (3.57 g, 30.0 mmol) in DMF (10 mL) at 0° C. and the mixture was stirred at rt for 2 h. To the reaction mixture was added a solution of diiodomethane (7.5 mL, 90.0 mmol) in DMF (10 mL) slowly without light and the mixture was stirred at rt for 20 h. The mixture was then quenched with water and filtered. The filtrate was extracted with DCM (30 mL×6) and the combined organic layers were washed with brine (50 mL×3), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a yellow solid (4.47 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434695B2
Source datasetuspto-grants-2016_09
ORD IDord-4ac7af751afe4a0c8814018ded4486d1
Source noteuspto-grants-2016_09