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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091301Generated: October 31, 2026

Methyl iodide → 1-(5-chloro-1-methyl-1H-indol-2-yl)heptan-1-one

https://huagongshe.com/reaction/2091301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 66777278HCID 66777278—
SolventDimethylformamideHCID 6228—
Product1-(5-chloro-1-methyl-1H-indol-2-yl)heptan-1-oneHCID 6677776835%

Reaction Steps

To a solution (10 mL) of 1-(5-chloro-1H-indol-2-yl)heptan-1-one (1.00 g) synthesized in Example A106(2) in N,N-dimethylformamide was added sodium hydride (60%, oily, 182 mg) at 0° C. and the mixture was stirred under argon atmosphere for 30 min. After stirring, methyl iodide (354 μL) was added. The reaction mixture was stirred at room temperature overnight, saturated aqueous ammonium chloride solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was washed with hexane to give the title object compound (367 mg, 35%) as a pale-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-b0737de42eb240fdb6c852451d574ebb
Source noteuspto-grants-2013_05