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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748255Generated: October 30, 2026

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

https://huagongshe.com/reaction/1748255

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 6723497790.4%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a stirred solution of thionyl chloride (4.1 mL, 56.8 mmol) in acetonitrile (30 mL) cooled to −45° C. is added a solution of tert-butyl (3-hydroxybutan-2-yl)carbamate (4.30 g, 22.7 mmol) in acetonitrile (40 mL) by syringe over 10 min, keeping the internal temperature below −40° C. When the addition is complete, 4-dimethylamino pyridine (277.5 mg, 2.3 mmol) is added followed by the dropwise addition of pyridine (9.2 mL, 113.6 mmol), keeping the temperature below −40° C. The reaction mixture is stirred at −40° C. for 1 h. 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 crude compound (4.83 g, 90%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150577B2
Source datasetuspto-grants-2015_10
ORD IDord-d0ebf89da1bc49668cc2af72baf308cd
Source noteuspto-grants-2015_10