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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247369Erstellt: 24. Oktober 2026

Methyl acetoacetate → Ammonia

https://huagongshe.com/de/reaction/247369

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl acetoacetateHCID 7757—
EduktPiperidineHCID 8082—
Edukt2,1,3-Benzoxadiazole-4-carbaldehydeHCID 10290873—
Edukt3-Aminocrotonic acid-(2-dimethylaminoethyl)esterHCID 12529187—
Edukt2-Acetyl-3-benzofurazan-4-yl-acrylic acid methyl esterHCID 53433213—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelBenzeneHCID 241—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktAmmoniaHCID 222—
Produkt2-(Dimethylamino)ethyl 3-oxobutanoateHCID 12529170—

Reaktionsschritte

2,1,3-Benzoxadiazol-4-carbaldehyde is reacted with aceto-acetic acid methyl ester in benzene in the presence of catalytic amounts of piperidine and acetic acid. The resultant 2-acetyl-3-(2,1,3-benzoxadiazol-4-yl)-2-propenoic acid methyl ester (crystalline, mixture of Z and E isomers) is cyclized in dioxane under refluxing with an equivalent amount of 3-aminocrotonic acid-(2-dimethylaminoethyl)ester {M.P. 56°; obtained by reaction of aceto-acetic acid-(2-dimethylaminoetyl)ester [B.P.0.01 mm 140°-150°, obtained by reaction of diketen with 2-dimethylaminoethanol at 70°], with ammonia gas at 60°}, to give 4-(2,1,3-benzoxadiazol-4-yl)-1,4-dihydro-5-methoxycarbonyl-2,6-dimethyl-3-pyridine carboxylic acid-(2-dimethylaminoethyl)ester (M.P. 161°).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04707482
Quelldatensatzuspto-grants-1987_11
ORD IDord-f29eca7ed8a44004bccdb125e00b9758
Quellennotizuspto-grants-1987_11