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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 557973Erstellt: 24. Oktober 2026

Tetrahydrofuran → Benzyl 3-(1,1-dimethylprop-2-en-1-yl)-3-hydroxypyrrolidine-1-carboxylate

https://huagongshe.com/de/reaction/557973

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt2-Butene, 1-bromo-3-methyl-HCID 70092—
Edukt1-N-Cbz-3-pyrrolidinoneHCID 561203—
KatalysatorZincHCID 23994—
LösungsmittelAmmonium ChlorideHCID 25517—
ProduktBenzyl 3-(1,1-dimethylprop-2-en-1-yl)-3-hydroxypyrrolidine-1-carboxylateHCID 66662637—

Reaktionsschritte

To a suspension of benzyl 3-oxopyrrolidine-1-carboxylate (4.50 g, 0.0205 mol) and 4-bromo-2-methyl-2-butene (4.75 mL, 0.0412 mol) in 25.0 mL of saturated ammonium chloride and tetrahydrofuran (4.75 mL, 0.0586 mol) was added zinc (2.70 g, 0.0412 mol) at rt. Soon after stirring was started, gas and heat were evolved. After 45 min., the resulting light grey mixture was filtered through celite. Layers of the filtrate were separated and the aqueous layer of the filtrate was extracted with EtOAc. The organic layers were combined, washed with brine, dried and evaporated in-vacuo. The residue was purified on silica gel, eluting with 0 to 40% EtOAc in hexane, to give the desired product. LCMS (M+Na) 290.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08058288B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-65b6b597bfa9482c91ad92277f821fd0
Quellennotizuspto-grants-2011_11