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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59197Generated: October 29, 2026

(Diethylamino)sulfur trifluoride → HCID 67153916, compound

https://huagongshe.com/reaction/59197

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantHCID 67153941HCID 67153941—
SolventDichloromethaneHCID 6344—
ProductHCID 67153916HCID 671539167%

Reaction Steps

To a solution of {(1S,2S,3S,4R,5S)-2,3,4-Tris-benzyloxy-5-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-6,8-dioxa-bicyclo[3.2.1]oct-1-yl}-methanol (616 mg, 0.871 mmol) in dichloromethane (3 mL) at 0 degrees Celsius was added diethylaminosulfur trifluoride (170 microL, 1.3 mmol) and the resulting mixture was slowly warmed to room temperature and stirred at this temperature for 16 hours. The mixture was diluted with dichloromethane and washed with a saturated solution of aqueous sodium bicarbonate, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography over silica gel using a 40 g redisep silica cartridge (eluting with a gradient of 0 to 20% ethyl acetate in heptane) to afford (1S,2S,3S,4R,5S)-2,3,4-tris-benzyloxy-5-[4-chloro-3-(4-ethoxy-benzyl)-phenyl]-1-fluoromethyl-6,8-dioxa-bicyclo[3.2.1]octane as a colorless oil (40 mg, 7% yield). (LCMS) 753.4 (M+HCOO−: negative mode).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439901B2
Source datasetuspto-grants-2016_09
ORD IDord-9637fb12066843d6a1232f15fdf0d6e7
Source noteuspto-grants-2016_09