Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559719Generated: October 30, 2026

tert-Butylsulfinamide, (R)-(+)- → HCID 87126736, compound

https://huagongshe.com/reaction/559719

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (R)-(+)-HCID 10964479—
Reactant3-Bromo-1,2-oxazole-5-carbaldehydeHCID 14880838—
CatalystTitanium isopropoxideHCID 11026—
SolventDichloromethaneHCID 6344—
ProductHCID 87126736HCID 87126736—

Reaction Steps

To a solution of 3-bromo-isoxazole-5-carbaldehyde (182 mg, 1.03 mmol) and (R)-(+)-2-methyl-2-propanesulfinamide (150 mg, 121 mmol) in CH2Cl2 (2 mL) was added titanium (IV) isopropoxide (0.667 mL, 2.28 mmol) and the mixture was warmed at reflux. After 22 hours, the solvent was concentrated in vacuo and the remaining solution was diluted with EtOAc (33 mL) and saturated aqueous NaCl (6 mL) was added. The resultant heterogeneous mixture was stir at room temperature. After 30 minutes, the 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)-meth-(E)-ylideneamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063065B2
Source datasetuspto-grants-2011_11
ORD IDord-ad387e8917a849aa969a0a311f71c40a
Source noteuspto-grants-2011_11