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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358881Erstellt: 26. Oktober 2026

Water → tert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylate

https://huagongshe.com/reaction/358881

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukttert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylateHCID 5148195—
LösungsmittelChloroformHCID 6212—
Produkttert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 1010388058,8%

Reaktionsschritte

2.96 g (0.012 mole) of 70% aqueous m-chloroperbenzoic acid were added to a solution of 1.69 g (0.01 mole) of 1-t-butoxycarbonyl-3-pyrroline [prepared as described in Step (a) above] in 10 ml of chloroform, whilst ice-cooling, and the mixture was stirred with ice-cooling for 8 hours and then with water-cooling for 15 hours. At the end of this time, the reaction mixture was extracted with toluene and the extract was washed, in turn, with an aqueous solution of sodium bicarbonate, a 0.1N aqueous solution of sodium thiosulfate and water. It was then dried over anhydrous sodium sulfate, and the solvent was removed by evaporation under reduced pressure. The residue was subjected to silica gel column chromatography eluted with a 1:5 by volume mixture of ethyl acetate and toluene, to afford 1.09 g of 1-t-butoxycarbonyl-3,4-epoxypyrrolidine as a colorless oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04997943
Quelldatensatzuspto-grants-1991_03
ORD IDord-3b5843a477ee452f954ed9e0b498034d
Quellennotizuspto-grants-1991_03