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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549105Generated: October 30, 2026

(Diethylamino)sulfur trifluoride → tert-butyl (4R)-4-(1-fluoro-1-methylethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate

https://huagongshe.com/reaction/549105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantTert-butyl (R)-4-(2-hydroxypropan-2-YL)-2,2-dimethyloxazolidine-3-carboxylateHCID 11379920—
SolventDichloromethaneHCID 6344—
Producttert-butyl (4R)-4-(1-fluoro-1-methylethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylateHCID 6715747551.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

tert-Butyl (4R)-4-(1-hydroxy-1-methylethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (3.80 g, 14.7 mmol), prepared by the method of Joullie, Tetrahedron, 52, pp. 11673-11694, (1996) was dissolved in 90 mL of anhydrous CH2Cl2. The solution was cooled to −78° C. under an atmosphere of N2. (Diethylamino)sulfur trifluoride (DAST) (2.25 mL, 17.0 mmol) was added and the reaction was allowed to warm to ambient temperature overnight. The reaction was quenched with saturated NaHCO3 solution and the layers were separated. The organic portion was washed successively with H2O and brine, dried over Na2SO4 and concentrated under reduced pressure. Chromatography (SiO2, 7% EtOAc/hexanes) gave tert-butyl (4R)-4-(1-fluoro-1-methylethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (1.98 g) as a nearly colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943609B2
Source datasetuspto-grants-2011_05
ORD IDord-869a5e740d8749d88e84bbaed4a01031
Source noteuspto-grants-2011_05