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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388752Generated: October 27, 2026

(Diethylamino)sulfur trifluoride → methyl (2E)-((3R,5S)-3-{[tert-butyl(diphenyl)silyl]oxy}-5-fluoro-4-methylenecyclohexylidene)acetate

https://huagongshe.com/reaction/388752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantMethyl (2z)-((3r,5r)-3-{[tert-butyl(diphenyl)silyl]oxy}-5-hydroxy-4-methylenecyclohexylidene)acetateHCID 131730230—
SolventDichloromethaneHCID 6344—
Productmethyl (2E)-((3R,5S)-3-{[tert-butyl(diphenyl)silyl]oxy}-5-fluoro-4-methylenecyclohexylidene)acetateHCID 131730231—

Reaction Steps

The compound of Example 18A (600 mg, 0.23 mmol) was dissolved in 2.4 mL of dichloromethane, and the resultant solution was cooled to −78° C. (Diethylamino)sulfur trifluoride (DAST, 0.6 mL) was added; the mixture was stirred for 30 minutes, and then quenched by addition of saturated aqueous sodium bicarbonate solution. The mixture was warmed to ambient temperature; the organic phase was dried over Na2SO4. The solvents were removed in vacuo; the residue was purified by chromatography on an Analogix IntelliFlash 280™, eluting with a gradient of 5% to 7% ethyl acetate in hexanes, to give the titled compound, plus some mixed fractions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377913B2
Source datasetuspto-grants-2013_02
ORD IDord-2d7b677769144990881525cd99d121c5
Source noteuspto-grants-2013_02