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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886957Generated: November 1, 2026

Methyl iodide → 1-Methyl-6-nitro-2-phenyl-1H-indole

https://huagongshe.com/reaction/1886957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant18-Crown-6HCID 28557—
Reactant6-Nitro-2-phenyl-1H-indoleHCID 20759801—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product1-Methyl-6-nitro-2-phenyl-1H-indoleHCID 2143250999.1%

Reaction Steps

To a solution of 6-nitro-2-phenyl-1H-indole (106 mg, 0.44 mmol) and 18-Crown-6 (130 mg, 0.49 mmol) in anhydrous tetrahydrofuran (2 mL) at room temperature was added potassium tert-butoxide (55 mg, 0.49 mmol) followed by methyl iodide (31 μL, 0.49 mmol). The solution was stirred at room temperature for 30 min. Tetrahydrofuran was removed in vacuo. Ethyl acetate was added, and the organic layer was washed with water and then brine. The combined organic layers were dried over anhydrous MgSO4 and evaporated to afford 110 mg (98%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501713B2
Source datasetuspto-grants-2013_08
ORD IDord-46d8a0afe34a495197eadb022b12630e
Source noteuspto-grants-2013_08