Reaktion #11801

Reaktionsgleichung

(2-Amino-ethyl)-carbamic acid tert-butyl ester

4-fluorobenzaldehyde

triethylamine

magnesium sulfate

sodium borohydride

→

title compound

Ausbeute 75.2%

[2-(4-fluoro-benzylamino)-ethyl]-carbamic acid tert-butyl ester

Ausbeute 75.2%

Lösungsmittel

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAfter 2 h the reaction was quenched with water
2. 2
   Extraktionextracted three times with ethyl acetate
3. 3
   WaschenThe combined organic layers were washed three times with water
4. 4
   Extraktionthe desired product extracted into the aqueous layer with 0.5 M hydrochloric acid (4×50 mL)
5. 5
   WaschenThe combined acid wash
6. 6
   Temperaturwas cooled to 0° C.
7. 7
   ExtraktionThe aqueous layer was extracted three times with chloroform
8. 8
   Waschenthe combined chloroform layer washed three times with water
9. 9
   Trocknendried over sodium sulfate
10. 10
    Einengenconcentrated

Vorschrift

(2-Amino-ethyl)-carbamic acid tert-butyl ester (5.95 g, 37.1 mmol), 4-fluorobenzaldehyde (5.07 g, 40.9 mmol, 4.4 mL), triethylamine (1.50 g, 14.9 mmol, 2.1 mL) and magnesium sulfate (6.71 g, 55.7 mmol) were stirred in methanol (50 mL). After 1.5 h the solution was cooled to 0° C. and sodium borohydride (8.4 g, 223 mmol) was added in portions. After 2 h the reaction was quenched with water and extracted three times with ethyl acetate. The combined organic layers were washed three times with water and the desired product extracted into the aqueous layer with 0.5 M hydrochloric acid (4×50 mL). The combined acid wash was cooled to 0° C. and basified with saturated aqueous ammonium hydroxide. The aqueous layer was extracted three times with chloroform and the combined chloroform layer washed three times with water, dried over sodium sulfate and concentrated to yield the title compound as a colorless oil (7.49 g).

Quelle