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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1762457Erstellt: 26. Oktober 2026

Dicyclohexylcarbodiimide → 2-Pyrrolidinone, 1-((4-chlorophenyl)sulfonyl)-

https://huagongshe.com/reaction/1762457

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt4-{[(4-Chlorophenyl)sulfonyl]amino}butanoic acidHCID 2053482—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Pyrrolidinone, 1-((4-chlorophenyl)sulfonyl)-HCID 66753591,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In 20 ml of tetrahydrofuran was dissolved 2.78 g of N-(4'-chlorobenzenesulfonyl)-4-aminobutyric acid (0.01 mole). To the stirred solution on an ice bath was added 2.06 g of dicyclohexylcarbodiimide (0.01 mole), and the mixture was stirred at 0° C. for 21 hours. The reaction mixture was filtered, and the solid material was washed with anhydrous tetrahydrofuran. The filtrate and the washings were combined, and tetrahydrofuran was removed under reduced pressure. The residue thus obtained was recrystallized from a mixed solvent of chloroform-ether to give 2.37 g of N-(4'-chlorobenzenesulfonyl)-2-pyrrolidone as crystals. Physical properties were identical with those in Synthetic Example 3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04833156
Quelldatensatzuspto-grants-1989_05
ORD IDord-4e17afe515de4ed6bdec791d6f3984de
Quellennotizuspto-grants-1989_05