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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521707Generated: October 30, 2026

Hydrochloric Acid → Tert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2,2-dioxide

https://huagongshe.com/reaction/1521707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium periodateHCID 23667635—
ReactantTert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2-oxideHCID 67235111—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2,2-dioxideHCID 8668238861%

Reaction Steps

The crude tert-butyl 6-methyl-1,2,3-oxathiazinane-3-carboxylate 2-oxide (2.52 g, 10.7 mmol) is dissolved in acetonitrile (25 mL) and H2O (15 mL) is added. The solution is cooled in an ice bath and sodium periodate (3.4 g, 16.1 mmol) is added in one portion. After 5 min, the pH is adjusted to 7-8 by addition of saturated Na2HPO4 solution. Then RuCl3 (22 mg, 0.11 mmol) in H2O (0.5 mL) is added. The pH is kept between 6 and 9 by addition of Na2HPO4 solution. After 2 h, H2O (100 mL) is added and pH is adjusted to 6 by addition of 2M HCl solution. The reaction mixture is extracted with EtOAc and the organic layer is washed with NaHCO3 and brine and the washes are back extracted once with EtOAc. The combined organic layers are dried (MgSO4), filtered and concentrated. The crude product is purified via by flash column chromatography using a gradient elution of 5-80% ethyl acetate/hexanes which affords the title compound (1.63 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073926B2
Source datasetuspto-grants-2015_07
ORD IDord-cacac27ea98540c88cba1e3deed6a078
Source noteuspto-grants-2015_07