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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1513376Erstellt: 25. Oktober 2026

Acetic Acid → Pentyl 2-(3-chloro-2-pyridinyl)-5-oxopyrazolidine-3-carboxylate

https://huagongshe.com/reaction/1513376

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1-PentanolHCID 6276—
Edukt3-Chloro-2-hydrazinylpyridineHCID 556100—
EduktDimethyl maleateHCID 5271565—
EduktSodiumHCID 5360545—
LösungsmittelWaterHCID 962—
ProduktPentyl 2-(3-chloro-2-pyridinyl)-5-oxopyrazolidine-3-carboxylateHCID 5954945042%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a three-necked flask, pentan-1-ol (150 mL) was added. And the sodium (3.0 g, 0.13 mol) was added partially. The reaction mixture was heated to reflux for 30 minutes at 100° C. When the sodium reacted completely, the mixture was cooled to 60° C. Then 3-chloro-2-hydrazinylpyridine (12.75 g, 98%, 0.09 mol) were added and reacted for 30 minutes. The dimethyl maleate (12.50 g, 0.11 mol) was added dropwise. The reaction mixture was heated to reflux for 10 minutes. After cooled to 65° C., the reaction mixture was neutralized with glacial acetic acid (13.04 g, 0.23 mol) and diluted with water (300 mL). After cooled to room temperature, solid is separated out to be filtered and, washed with 40% aqueous solution of ethanol (3×50 mL) and dried to give pentyl 2-(3-chloro-2-pyridinyl)-5-oxopyrazolidine-3-carboxylate (12.00 g) as a orange solid in 42% yield. HPLC area normalization method content is 95% (Analytical condition: chromatographic column: ZORBAX Eclipse XDB-C8 4.6×150 mm 5 μm, mobile phase:the ratio of acetonitrile to water is 70:30).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08217179B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-f73c69cd99274b18a58ee56e06f775ef
Quellennotizuspto-grants-2012_07