Reaktion #167090

Reaktionsgleichung

(S)-benzyl 1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-oxopyrrolidine-2-carboxylate

p-toluene sulfonic acid monohydride

ethylene glycol

→

(S)-benzyl 7-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-1,4-dioxa-7-azaspiro[4.4]nonane-8-carboxylate

Lösungsmittel

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthe mixture was refluxed for 18 hours
2. 2
   Sonstigeremoving the generated byproduct water with a Dean-Stark apparatus
3. 3
   workup.ADDITIONThe crude mixture was then diluted with ethyl acetate
4. 4
   Waschenwashed
5. 5
   Trocknendried over sodium sulfate
6. 6
   Einengenconcentrated down on rotovap
7. 7
   SonstigeThe crude residue was then purified on normal phase column chromatography with 5% MeOH/DCM

Vorschrift

(S)-benzyl 1-((S)-2-(methoxycarbonylamino)-3-methylbutanoyl)-4-oxopyrrolidine-2-carboxylate (2.45 g, 6.51 mmol) in a round bottom flask was dissolved in anhydrous toluene (200 mL) and p-toluene sulfonic acid monohydride (124 mg, 0.1 mmol) and ethylene glycol (808 mg, 13.02 mmol) were added and the mixture was refluxed for 18 hours, removing the generated byproduct water with a Dean-Stark apparatus. The crude mixture was then diluted with ethyl acetate and washed, respectively, with 10% citric acid, saturated ammonium chloride, 10% sodium carbonate and finally with brine. The organic layers were combined and dried over sodium sulfate and concentrated down on rotovap. The crude residue was then purified on normal phase column chromatography with 5% MeOH/DCM. (2.3 g, 84%)

Quelle