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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093039Generated: October 29, 2026

Methyl iodide → 4-Fluoro-2-(4,4,5-trimethyl-1,1-dioxido-1,2,5-thiadiazolidin-2-yl)benzonitrile

https://huagongshe.com/reaction/1093039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-(4,4-Dimethyl-1,1-dioxido-1,2,5-thiadiazolidin-2-yl)-4-fluorobenzonitrileHCID 57904973—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Fluoro-2-(4,4,5-trimethyl-1,1-dioxido-1,2,5-thiadiazolidin-2-yl)benzonitrileHCID 57904951100.1%

Reaction Steps

To a solution of 2-(4,4-dimethyl-1,1-dioxido-1,2,5-thiadiazolidin-2-yl)-4-fluorobenzonitrile (3.18 g, 11.81 mmol) in DMF (40 mL) was added NaH (0.312 g, 12.99 mmol) and the mixture stirred for 5 min. Iodomethane (1.477 mL, 23.62 mmol) was added and the mixture stirred at 90° C. for 2 h then at room temperature for 16 h. The mixture was diluted with H2O and extracted with ethyl acetate. The organic phase was washed two times with H2O followed by brine, dried (Na2SO4), filtered and concentrated to give the title compound as a white solid (3.35 g, 100% yield). LCMS (M+H) calcd for C12H15FN3O2S: 284.08; found: 284.14. 1H NMR (300 MHz, CDCl3) δ: 7.70-7.61 (2H, m), 7.11-7.05 (1H, m), 3.80 (2H, s), 2.73 (3H, s), 1.42 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129398B2
Source datasetuspto-grants-2012_03
ORD IDord-94a8b135ff974b0fad4d9272571a95b8
Source noteuspto-grants-2012_03