Reaktion #163456

Reaktionsgleichung

iodine

pyridine

O-ethyl carbonisothiocyanatidate

t-butylamine

hexanal

→

title compound

Ausbeute 92.6%

ethyl [(5Z)-4-butyl-2-tert-butylisothiazol-5(2H)-ylidene]carbamate

Ausbeute 92.6%

Lösungsmittel

methanol

tetrahydrofuran

acetonitrile

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe solids were removed by vacuum filtration through a glass frit
2. 2
   Einengenthe liquor was concentrated by rotary evaporator
3. 3
   Sonstigeto give the crude imine as a pale yellow oil
4. 4
   workup.ADDITIONwas added dropwise
5. 5
   workup.STIRRINGThe resulting yellow mixture was stirred at room temperature for 1 hour
6. 6
   Sonstigeto form a brown slurry
7. 7
   workup.STIRRINGThe mixture was stirred at room temperature for 2 hours
8. 8
   SonstigeThe excess iodine was quenched by addition of solid sodium metabisulfite until the mixture
9. 9
   workup.ADDITIONSaturated aqueous sodium bicarbonate solution was added
10. 10
    workup.STIRRINGthe mixture was stirred at room temperature for 15 minutes
11. 11
    ExtraktionThe mixture was extracted with dichloromethane (3×75 mL)
12. 12
    TrocknenThe combined organic extracts were dried (MgSO4)
13. 13
    Filtrationfiltered
14. 14
    Einengenconcentrated by rotary evaporator
15. 15
    Sonstigeto give a brown oil
16. 16
    SonstigeThe product was purified by flash chromatography (silica gel: 25-95% ethyl acetate in hexanes)

Vorschrift

To a solution of hexanal (Aldrich, 20.0 g, 200 mmol) in acetonitrile (20 mL) in a 100-mL, round-bottomed flask containing molecular sieves (10 g) was added neat t-butylamine (Aldrich, 16.1 g, 220 mmol). The mixture was stirred at room temperature overnight. The solids were removed by vacuum filtration through a glass frit and the liquor was concentrated by rotary evaporator to give the crude imine as a pale yellow oil. The crude imine was dissolved in anhydrous tetrahydrofuran (200 mL) containing pyridine (Aldrich, 15.8 g, 200 mmol) and O-ethyl carbonisothiocyanatidate (Aldrich, 15.7 g, 120 mmol) was added dropwise. The resulting yellow mixture was stirred at room temperature for 1 hour. Anhydrous methanol (100 mL) and iodine (Aldrich, 30.5 g, 120 mmol) were added to form a brown slurry. The mixture was stirred at room temperature for 2 hours. The excess iodine was quenched by addition of solid sodium metabisulfite until the mixture changed to yellow. Saturated aqueous sodium bicarbonate solution was added and the mixture was stirred at room temperature for 15 minutes. The mixture was extracted with dichloromethane (3×75 mL). The combined organic extracts were dried (MgSO4), filtered, and concentrated by rotary evaporator to give a brown oil. The product was purified by flash chromatography (silica gel: 25-95% ethyl acetate in hexanes) to afford 31.6 g (56%) of the title compound. 1H NMR (DMSO-d6) δ 0.90 (t, J=7.3 Hz, 3H), 1.22 (t, J=7.1 Hz, 3H), 1.23-1.36 (m, 2H), 1.50-1.60 (m, 2H), 1.55 (s, 9H), 2.51 (t, J=7.5 Hz, 2H), 4.10 (q. J=7.1 Hz, 2H), 8.45 (s, 1H); MS (ESI+) m/z 285 (M+H)+.

Quelle