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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660798Generated: October 29, 2026

Hydrochloric Acid → 5-[2-Benzyloxy-4-(2-methoxymethylbenzyl)-phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-one

https://huagongshe.com/reaction/660798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCesium fluorideHCID 25953—
Reactant5-[2-Benzyloxy-4-(2-methoxymethylbenzyl)-phenyl]-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-oneHCID 68839274—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-[2-Benzyloxy-4-(2-methoxymethylbenzyl)-phenyl]-1,1-dioxo-1,2,5-thiadiazolidin-3-oneHCID 68838509—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 5-[2-benzyloxy-4-(2-methoxymethylbenzyl)-phenyl]-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (375 mg, 0.679 mmol) in DMF (5 mL) is added CsF (361 mg, 2.37 mmol) and the mixture is stirred at 65° C. for 3 h. The mixture is diluted with EtOAc and water then is acidified with 1N HCl. The organic phase is washed with 1N HCl, water and brine. The organic phase is dried over sodium sulfate and the solvent is removed under reduced pressure to give the title compound as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-96e1e06e275d47c7ac8136df3d3af949
Source noteuspto-grants-2011_12