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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | 3-Cyanophenol | HCID 13394 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Nitro-1H-indole | HCID 78502 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-((6-nitro-1H-indol-1-yl)methoxy)benzonitrile | HCID 90030447 | 51% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434695B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-4ac7af751afe4a0c8814018ded4486d1 |
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| Source note | uspto-grants-2016_09 |
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