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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984561Generated: October 30, 2026

2-Methylindole → HCID 21940686, compound

https://huagongshe.com/reaction/984561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylindoleHCID 7224—
Reactant1-Iodo-3,5-dimethylbenzeneHCID 140924—
ProductHCID 21940686HCID 2194068695%

Reaction Steps

Using general procedure A, 2-methylindole (165 mg, 1.26 mmol)) was coupled with 5-iodo-m-xylene (150 μL, 1.04 mmol). The crude product was purified by flash chromatography on silica gel (2×15 cm; hexane-ether 40:1; 15 mL fractions). Fractions 4-9 provided 232 mg (95% yield) of the product as a colorless oil. 1H NMR (300 MHz, CDCl3): δ 7.62-7.53 (m, 1H), 7.15-7.05 (m, 4H), 6.98 (s, 2H), 6.39 (s, 1H), 2.41 (s, 6H), 2.31 (d, J=1.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867298B2
Source datasetuspto-grants-2005_03
ORD IDord-6397036db79843ff8ae10f1e95901474
Source noteuspto-grants-2005_03