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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 850637Erstellt: 26. Oktober 2026

Benzaldehyde → 3-(2,1,3-Benzothiadiazol-5-yl)-4-benzyl-5-hydroxy-5-(4-methoxy-phenyl)-5H-furan-2-one

https://huagongshe.com/reaction/850637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktPotassium CarbonateHCID 11430—
EduktBenzenamine, N-sulfinyl-HCID 70739—
EduktSodiumHCID 5360545—
EduktEthyl 2-(2,1,3-benzothiadiazol-5-yl)-4-(4-methoxyphenyl)-4-oxobutanoateHCID 10926758—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelAcetoneHCID 180—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
Produkt3-(2,1,3-Benzothiadiazol-5-yl)-4-benzyl-5-hydroxy-5-(4-methoxy-phenyl)-5H-furan-2-oneHCID 15410455—

Reaktionsschritte

0.38 g of benzaldehyde and 120 g of ethyl 2-(2,1,3-benzothiadiazol-5-yl)-4-(4-methoxyphenyl)-4-oxo-butanoate ("A"), m.p. 89°, (obtainable by reaction of 5.5 g of ethyl 2-(2,1,3-benzothiadiazol-5-yl) acetate with 5.5 g of 2'-bromo-4-methoxyacetophenone and 4 g of potassium carbonate in 200 ml of acetone, 18 hours under reflux; ethyl 2-(2,1,3-benzothiadiazol-5-yl) acetate, m.p. 40-41°, is obtained by reaction of 24.3 g of ethyl 3,4-diaminophenyl acetate and 26.9 ml of thionylaniline in 80 ml of toluene, 4 hours under reflux) are added to a solution of 80 mg of sodium in 5 ml of methanol and the mixture is heated under reflux for one hour. After addition of 5 ml of acetic acid, it is heated for a further 16 hours. The solvent is removed and the residue is worked up in the customary manner. 3-(2,1,3-Benzothiadiazol-5-yl)-4-benzyl-5-hydroxy-5-(4-methoxy-phenyl)-5H-furan-2-one, FAB 431, is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06017939
Quelldatensatzuspto-grants-2000_01
ORD IDord-7de4d829c5034304a9251f258cd56006
Quellennotizuspto-grants-2000_01