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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 660543Erstellt: 26. Oktober 2026

Imidazole → 5-(2-Benzyloxy-4-iodomethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one

https://huagongshe.com/reaction/660543

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktIodineHCID 807—
EduktTriphenylphosphineHCID 11776—
Edukt5-(2-Benzyloxy-4-hydroxymethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-oneHCID 66756654—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(2-Benzyloxy-4-iodomethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-oneHCID 66756809—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a 0° C. slurry of resin-bound PPh3 (850 mg, 2.5 mmol) in CH2Cl2 (10 mL) in a pressure vessel is added imidazole (200 mg, 2.8 mmol) and iodine (650 mg, 2.5 mmol). The mixture is vigorously stirred at 0° C. for 30 min. To the mixture is added a solution of 5-(2-benzyloxy-4-hydroxymethylphenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (550 mg, 1.2 mmol) in CH2Cl2 (10 mL) dropwise. The vessel is sealed and heated to 45° C., with stirring, for 2 h. The reaction is allowed to cool to RT and the mixture is filtered through a plug of cotton to remove the resin. The organic solution is washed with sat. Na2SO3 and brine, then dried over MgSO4. The solvent is removed under reduced pressure to afford the title compound as a white solid which is used in the next step without further purification: (M+H)+=576.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084448B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-e414390b6c7b4237afa1d6e317f7f2ea
Quellennotizuspto-grants-2011_12