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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361215Generated: October 30, 2026

tert-Butylsulfinamide, (R)-(+)- → (NE)-N-[1-(3-bromo-1,2-oxazol-5-yl)propylidene]-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1361215

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
Reactant1-(3-Bromo-5-isoxazolyl)-1-propanoneHCID 13802101—
CatalystTitanium isopropoxideHCID 11026—
SolventDichloromethaneHCID 6344—
Product(NE)-N-[1-(3-bromo-1,2-oxazol-5-yl)propylidene]-2-methylpropane-2-sulfinamideHCID 87126762—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 1-(3-bromo-isoxazol-5-yl)-propan-1-one (452 mg, 2.22 mmol) and (R)-(+)-2-methyl-2-propanesulfinamide (342 mg, 2.82 mmol) in CH2Cl2 (5 mL) was added titanium (IV) isopropoxide (1.4 mL, 4.9 mmol) and the mixture was warmed at 45° C. After 24 hours, the reaction was monitored by LC-MS, and the solvent was concentrated in vacuo and the remaining residue was diluted with EtOAc (32 mL) and saturated aqueous NaCl (8 mL) was added. The heterogeneous mixture was filtered through a pad of diatomaceous earth. The EtOAc layer was dried over Na2SO4, filtered and concentrated in vacuo. The crude material was purified by silica gel chromatography eluting with a gradient of 0-100% EtOAc in heptane to afford 2-methyl-propane-2-sulfinic acid [1-(3-bromo-isoxazol-5-yl)-prop-(E)-ylidene]-amide. MS m/z 307 (M), 309 (M+2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879873B2
Source datasetuspto-grants-2011_02
ORD IDord-ef69969295554abd838feedff6dca926
Source noteuspto-grants-2011_02