Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158245Generated: November 2, 2026

Water → HCID 67426478, compound

https://huagongshe.com/reaction/1158245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-MethylmorpholineHCID 7972—
ReactantThionyl ChlorideHCID 24386—
Reactant(2S)-2-(propylamino)pentan-1-olHCID 55300429—
SolventDichloromethaneHCID 6344—
ProductHCID 67426478HCID 6742647879%

Reaction Steps

N-Methylmorpholine (27.3 mL) was added to a solution of (S)—N-propylnorvalinol (11.5 g) in dichloromethane (200 mL) under stirring at room temperature. A solution of thionyl chloride (9.32 mL) in dichloromethane (64 mL) was added dropwise to the resulting light yellow solution under ice-cooling and stirring. The resulting suspension was stirred at room temperature. Water was added to the suspension under ice-cooling and stirring, and the mixture was extracted with dichloromethane. The organic layer was washed with an aqueous 1 mol/L hydrochloric acid solution and subsequently with a saturated aqueous sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate, and then the solvent was removed by distillation under reduced pressure. The residue was dried under reduced pressure at room temperature overnight to give (S)-3,4-dipropyl-1,2,3-oxathiazolidine 2-oxide as a colorless oil (16.1 g, 79% yield, cis:trans=about 38:62 determined from the integration ratio in 1H-NMR).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807840B2
Source datasetuspto-grants-2010_10
ORD IDord-109ca6becbf94111835bfb07f92c7ca4
Source noteuspto-grants-2010_10