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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818618Generated: November 3, 2026

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

https://huagongshe.com/reaction/1818618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 66777278HCID 66777278—
SolventDimethylformamideHCID 6228—
Product1-(5-chloro-1-methyl-1H-indol-2-yl)heptan-1-oneHCID 66777768—

Reaction Steps

To a solution of the title compound of Example 1 Step B (98.0 mg, 0.37 mmol) in DMF was added NaH (15.0 mg, 60% suspension in mineral oil, 0.37 mmol). After 10 min, iodomethane (0.023 mL, 0.37 mmol) was added, and the mixture was stirred for 2 h, whereupon it was quenched by addition of sat. aq. NaHCO3. The aqueous phase was extracted with EtOAc, and the organic phase was concentrated in vacuo. Purification by flash chromatography on silica gel (0 to 10%, then 10 to 100% EtOAc in hexanes) provided the title compound: LCMS C, tr=2.78 min, m/z 278.3 [M+H]+; 1H NMR (500 MHz, CDCl3) δ 7.65 (app t, J=1.0 Hz, 1H), 7.31 (d, J=1.0 Hz, 2H), 7.20 (s, 1H), 4.05 (s, 3H), 2.95 (t, J=7.0 Hz, 2H), 1.79-1.72 (m, 2H), 1.43-1.26 (m, 6H), 0.90 (t, J=7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598398B2
Source datasetuspto-grants-2009_10
ORD IDord-516fbe1fbccd48d7b020e381d331f554
Source noteuspto-grants-2009_10