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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1697718Erstellt: 26. Oktober 2026

Isopropyl Acetate → 5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/1697718

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropyl AcetateHCID 7915—
EduktTriethylamineHCID 8471—
EduktPhenyl vinyl sulfoneHCID 79664—
EduktLithium BromideHCID 82050—
EduktHCID 178472689HCID 178472689—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(4-tert-Butylphenyl)-4-(phenylsulfonyl)pyrrolidine-2-carboxylic Acid Ethyl EsterHCID 667708288%

Reaktionsschritte

To a stirred solution of (E)-ethyl 2-(4-tert-butylbenzylideneamino)acetate (226 mg, 914 umol; example 441a) in THF (5 ml) under an argon atmosphere were added lithium bromide (119 mg, 1.37 mmol), triethylamine (191 ul, 1.37 mmol) and phenyl vinyl sulfone (154 mg, 914 umol; CAS Reg. No. 5535-48-8). The mixture was stirred at ambient temperature for 20 h. iPrOAc (50 ml) and ice water (40 ml) were added and the layers were separated. The organic layer was washed with brine (40 ml), dried over sodium sulfate and filtered. The solvent was removed under reduced pressure to give a yellow oil which was purified by column chromatography (silica gel, iPrOAc/n-heptane) to obtain the title compound (56 mg, 73 umol; 8%) as colorless solid. MS (ESI): m/z=416.2 [M+H]

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163793B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-4a5887a39fce47c6962960c891c32db4
Quellennotizuspto-grants-2012_04