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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234756Generated: October 25, 2026

(Diethylamino)sulfur trifluoride → tert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylate

https://huagongshe.com/reaction/2234756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(methylsulfinyl)phenyl]-1,3-oxazolidine-3-carboxylateHCID 68720168—
CatalystAntimony trichlorideHCID 24814—
SolventDichloromethaneHCID 6344—
Producttert-Butyl(4S,5R)-4-(fluoromethyl)-2,2-dimethyl-5-[4-(fluoromethylthio)phenyl]-1,3-oxazolidine-3-carboxylateHCID 6871963986.5%

Reaction Steps

A solution of diethylamino sulfurtrifluoride (DAST), (9.34 g, 1.75 eq) in 10 ml of dichloromethane was added drop wise to the solution of 14 (12.3 g) and antimony (III) chloride (0.23 g, 0.03 eq) in 150 ml of dichloromethane (anhydrous) at −5° C., and the reaction mixture was warmed up to room temperature overnight. A cold saturated solution of sodium bicarbonate (80 ml) was added and stirred for 30 min and extracted with dichloromethane (100 ml×2). The organic layer was washed with a 10% solution of sodium bicarbonate and with brine (50 ml) and dried over sodium sulfate. After purification, via a column, 10.7 g of the desired product (as a heavy oil) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713950B2
Source datasetuspto-grants-2010_05
ORD IDord-8b06519c7f18412d8da172fd10bbda06
Source noteuspto-grants-2010_05