Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598520Generated: October 25, 2026

Methyl iodide → 5,6-Difluoro-2-(methylsulfanyl)-1,3-benzothiazole

https://huagongshe.com/reaction/598520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178505403HCID 178505403—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5,6-Difluoro-2-(methylsulfanyl)-1,3-benzothiazoleHCID 4482010491.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension (0° C.) of 300 mg (1.476 mmol) 5,6-difluoro-benzothiazole-2-thiol and 306 mg (2.214 mmol) potassium carbonate in 6 mL N,N-dimethylformamide under nitrogen, were added 110.5 μL (1.77 mmol) iodomethane. The mixture was stirred at 0° C. for 1 h. The mixture was diluted with water (30 mL) and extracted with ethyl acetate. The combined extracts were washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo to provide 294 mg (91.7%) of the title compound as a solid. MS(m/e): 218.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897627B2
Source datasetuspto-grants-2011_03
ORD IDord-42fff5004a39426cbcdd2fc6075afefb
Source noteuspto-grants-2011_03