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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521711Generated: November 1, 2026

Pyridine → Tert-butyl 4,5-dimethyl-1,2,3-oxathiazolidine-3-carboxylate 2-oxide

https://huagongshe.com/reaction/1521711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantThionyl ChlorideHCID 24386—
Reactant3-(Boc-amino)-2-butanolHCID 541656—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 4,5-dimethyl-1,2,3-oxathiazolidine-3-carboxylate 2-oxideHCID 6723497790%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A stirred solution of thionyl chloride (4.1 mL, 56.8 mmol) in acetonitrile (30 mL) is cooled to −45° C. A solution of tert-butyl (3-hydroxybutan-2-yl)carbamate (4.3 g, 22.7 mmol) in acetonitrile (40 mL) is added by syringe over about 10 min, keeping the internal temperature below −40° C. When the addition is completed, 4-dimethylamino pyridine (278 mg, 2.3 mmol) is added. Then pyridine (9.2 mL, 114 mmol) is added dropwise by syringe, keeping the temperature below −40° C. The reaction mixture is stirred at −40° C. for 1 hr. Ethyl acetate (70 mL) is added to the suspension and the mixture is filtered at −35° C. The solid is washed with EtOAc and the filtrates are combined. Saturated Na2HPO4 solution (40 mL) is added and the mixture is stirred vigorously for 30 min. The organic layer is separated, washed with 1M NaHSO4, dried (MgSO4) and concentrated to afford the title compound (4.8 g, 90%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073926B2
Source datasetuspto-grants-2015_07
ORD IDord-91be77cdd80640c08b99a739bc5a4dfa
Source noteuspto-grants-2015_07