Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 378342Erstellt: 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/378342

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
PatentnummerUS06030990
Quelldatensatzuspto-grants-2000_02
ORD IDord-30b32bee0db848728b4ef299586b9700
Quellennotizuspto-grants-2000_02