Reaktion #305240

Reaktionsgleichung

hydrochloric acid

Di-tert-butyl dicarbonate

diethyl 3-(tert-butoxycarbonyl)-3-azabicyclo[3.3.0]octane-7,7-dicarboxylate

water

→

3-(tert-butoxycarbonyl)-3-azabicyclo[3.3.0]octane-7-carboxylic acid

Ausbeute 67.7%

Lösungsmittel

tert-butanol

Ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   Einengenconcentrated (12 N) hydrochloric acid (75 mL)
2. 2
   TemperaturThe mixture was heated
3. 3
   Temperaturat reflux for 8 h
4. 4
   SonstigeThe volatiles were evaporated
5. 5
   workup.DISSOLUTIONthe residue was dissolved in water (10 mL)
6. 6
   ExtraktionThe aqueous layer was extracted with ethyl acetate (200 mL)
7. 7
   WaschenThe organic layer was washed with water (2×200 mL) and brine (100 mL)
8. 8
   Trocknendried (anhydrous sodium sulfate)
9. 9
   Einengenconcentrated
10. 10
    Sonstige(rotary evaporation)
11. 11
    Sonstigepurified by silica gel column chromatography

Vorschrift

To the diethyl 3-(tert-butoxycarbonyl)-3-azabicyclo[3.3.0]octane-7,7-dicarboxylate (10.5 g, 29.5 mmol) was added water (25 mL) and concentrated (12 N) hydrochloric acid (75 mL). The mixture was heated at reflux for 8 h. The volatiles were evaporated, and the residue was dissolved in water (10 mL) and the pH of the solution was adjusted to pH 8 with 10% aqueous sodium bicarbonate. Di-tert-butyl dicarbonate (8.5 g, 39 mmol) in tert-butanol (60 mL) was added and the reaction was stirred overnight at ambient temperature. Ethyl acetate (100 mL) was added to the reaction and the pH of the solution was adjusted to pH 3 with 2 M aqueous hydrochloric acid. The aqueous layer was extracted with ethyl acetate (200 mL). The organic layer was washed with water (2×200 mL) and brine (100 mL), dried (anhydrous sodium sulfate), concentrated (rotary evaporation), and purified by silica gel column chromatography to give 5.1 g of 3-(tert-butoxycarbonyl)-3-azabicyclo[3.3.0]octane-7-carboxylic acid, as a white solid (1H NMR (CDCl3, 300 MHz): δ 3.59-3.40 (m, 2H), 3.36-3.05 (m, 2H), 3.02-2.76 (m, 2H), 2.65-2.60 (m, 1H), 2.24-2.04 (m, 2H), 1.85-1.66 (m, 2H), 1.46 (s, 9H); MS (m/z): 256 (M+1), 200 (M+1-56)).

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