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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 325420Erstellt: 25. Oktober 2026

Diethyl acetonedicarboxylate → Ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetate

https://huagongshe.com/reaction/325420

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl acetonedicarboxylateHCID 66045—
EduktSodium AcetateHCID 517045—
EduktHCID 178451312HCID 178451312—
KatalysatorZincHCID 23994—
LösungsmittelAcetic AcidHCID 176—
ProduktEthyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetateHCID 5403425631%

Reaktionsschritte

Crude t-butyl 5-(m-chlorophenyl)-2-hydroximino-3-oxopentanoate (43 g., 0.15 mol) and diethyl acetonedicarboxylate (28 ml, 30.3 g, 0.15 mol) are placed in a 1 liter round bottom flask and 250 ml of glacial acetic acid added. With stirring, 25 g (0.30 mol) anhydrous sodium acetate is added followed by 26 g Zn dust (94% fine, 0.364 mol) in a portionwise manner so that the exotherm does not bring the reaction to reflux. When addition is complete, the reaction is heated on a steam bath for one hour. The hot solution is then decanted from the residual zinc into 3 liters of ice water, and the resulting mixture is stirred vigorously until the oil solidifies. The mixture is then allowed to stand for 1.5 hours, and the solid is filtered. The solid is washed with water, dried in vacuo and recrystallized to give 21.5 g (31%) of ethyl 5-(t-butoxycarbonyl)-4-[2-(m-chlorophenyl)ethyl]-3-ethoxycarbonylpyrrole-2-acetate, M.P. 131°- 132°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04440779
Quelldatensatzuspto-grants-1984_04
ORD IDord-505488170c2b4d528249f20b4bfb6f2c
Quellennotizuspto-grants-1984_04