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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526530Generated: November 3, 2026

(Diethylamino)sulfur trifluoride → HCID 90389342, compound

https://huagongshe.com/reaction/1526530

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantHCID 13702272HCID 13702272—
SolventDichloromethaneHCID 6344—
ProductHCID 90389342HCID 9038934249.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (5-(chloromethyl)-4,5-dihydroisoxazol-3-yl)methanol (1.58 g, 10.56 mmol, 6a rac, Tetrahedron 1986, 42, 5267) in DCM (30 mL) at −78° C. was added (diethylamino)sulfur trifluoride (1.60 ml, 12.11 mmol). The reaction mixture was stirred at −78° C. for 10 min, warmed from −78° C. to room temperature over 15 min, stirred at room temperature for 1 h and quenched with saturated aq. saturated NaHCO3 solution. The reaction mixture was diluted with diethyl ether and water. The aqueous phase was extracted with diethyl ether (4×) and the combined organic extracts were washed with brine (1×), dried over MgSO4, filtered, and concentrated in vacuo to give a dark red oil. Purification by flash column chromatography on silica gel (20% diethyl ether in pentane) gave the title compound (0.79 g, 49% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085576B2
Source datasetuspto-grants-2015_07
ORD IDord-d8e0a3db4b41490c923ba3ca16b294a9
Source noteuspto-grants-2015_07