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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246635Generated: October 31, 2026

Methyl iodide → 3-iodo-1-methyl-5-(trifluoromethyl)-1H-indazole

https://huagongshe.com/reaction/246635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178506093HCID 178506093—
SolventTetrahydrofuranHCID 8028—
Product3-iodo-1-methyl-5-(trifluoromethyl)-1H-indazoleHCID 7128010579.3%

Reaction Steps

To a solution of 3-iodo-5-(trifluoromethyl)-1H-indazole (4.0 g, 12.8 mmol) in THF (80 mL) was added t-BuOK (2.0 g, 17.9 mmol) slowly at 0° C. and mixture stirred for 30 minutes, iodomethane (1.1 mL, 17.9 mmol) was added at 0° C., then warmed to room temperature and stirred for 1.5 hours, quenched with water (30 mL) and extracted with EtOAc (3×30 mL), the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The crude product was washed with ether (5 mL) and filtered to give 3-iodo-1-methyl-5-(trifluoromethyl)-1H-indazole (3.3 g, 79.3%) as a white solid. LCMS: (M+H)+=327.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-b169146a8fef4a42839ed2f594085684
Source noteuspto-grants-2014_02