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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279447Generated: October 30, 2026

Iodine → N-((3-fluoro-4-(trifluoromethoxy)phenyl)(oxazol-5-yl)methyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/2279447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-Bromo-2-fluoro-1-(trifluoromethoxy)benzeneHCID 2782217—
ReactantHCID 88924920HCID 88924920—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductN-((3-fluoro-4-(trifluoromethoxy)phenyl)(oxazol-5-yl)methyl)-2-methylpropane-2-sulfinamideHCID 86705473—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 4-bromo-2-fluoro-1-(trifluoromethoxy)benzene (582 g, 2247 mmol), Mg (54.6 g, 2247 mmol) and iodine in THF (10 mL) was heated at reflux for 2 h. The reaction was cooled to 0° C. and added to a solution of (E)-2-methyl-N-(oxazol-5-ylmethylene)propane-2-sulfinamide (300 g, 1498 mmol, step 1 of example 1) in toluene (10 mL) cooled to 0° C. The reaction was stirred at 0° C. for 30 min. The reaction was quenched with water and extracted with DCM. The organic layer was concentrated to afford crude N-((3-fluoro-4-(trifluoromethoxy)phenyl)(oxazol-5-yl)methyl)-2-methylpropane-2-sulfinamide (55) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133187B2
Source datasetuspto-grants-2015_09
ORD IDord-fb2f6f72ba314dacaefb342a25daac25
Source noteuspto-grants-2015_09