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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 611621Erstellt: 26. Oktober 2026

Methyl 5-(2,4-dioxothiazolidin-5-ylidene)methyl-2-methoxybenzoate → Methyl 5-(2,4-dioxothiazolidin-5-yl)methyl-2-methoxy-benzoate

https://huagongshe.com/reaction/611621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 5-(2,4-dioxothiazolidin-5-ylidene)methyl-2-methoxybenzoateHCID 54363563—
KatalysatorPalladiumHCID 23938—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 5-(2,4-dioxothiazolidin-5-yl)methyl-2-methoxy-benzoateHCID 992217861,3%

Reaktionsschritte

Methyl 5-(2,4-dioxothiazolidin-5-ylidene)methyl-2-methoxy-benzoate (9.52 g) was suspended into DMF (250 ml) and hydrogenated with 10% palladium/carbon (10.0 g) at room temperature under a hydrogen pressure of 3.5 kg/cm2. After the reaction, the solution was filtered and concentrated and water was added to the residue, which was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by means of silica gel column chromatography (developing solvent; methylene chloride:acetone=50:1) to obtain 5.88 g (61%) of aimed compound as an amorphous material.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06001862
Quelldatensatzuspto-grants-1999_12
ORD IDord-d5294bc744bd4cbcbdc7031cba19e279
Quellennotizuspto-grants-1999_12