Sulfuric Acid → 1-Methoxytricyclo[3.3.1.03,7]nonan-3-amine

HRID 1015559Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1015559
[CH3:1][O:2][C:3]12[CH2:11][CH:7]3[CH2:8][CH:9]([CH2:10]1)[C:5](C(O)=O)([CH2:6]3)[CH2:4]2.OS(O)(=O)=O.[N-:20]=[N+]=[N-].[Na+]>C(Cl)(Cl)Cl.O>[CH3:1][O:2][C:3]12[CH2:11][CH:7]3[CH2:8][CH:9]([CH2:10]1)[C:5]([NH2:20])([CH2:6]3)[CH2:4]2

Komponenten

6

Versuchsvorschrift

To the suspension of 1-methoxytricyclo[3.3.1.03,7]nonane-3-carboxylic acid obtained from step IV (0.39 g, 2.0 mmol) in CHCl3 (10 mL) was added conc. H2SO4 (1.0 mL, 20 mmol). Solid NaN3 (0.39 g, 6.0 mmol) was added in portions by keeping the reaction temperature below 40° C. After stirring at room temperature for 2 hrs, the reaction mixture was cooled to ice bath temperature, diluted with water and extracted with EtOAc. The aqueous layer was basified by adding 50% NaOH solution and extracted with CHCl3. The combined organic layer was washed with brine, dried over Na2SO4, and the solvent was removed under reduced pressure to obtain 1-methoxytricyclo[3.3.1.03,7]nonan-3-amine (0.23 g) in 69% yield. m/z (M+1) 168; 1H NMR (CDCl3) 300 MHz δ 3.27 (s, 3H), 2.40-2.34 (m, 1H), 2.16-2.08 (m, 1H), 1.97 (ddd, J=2.0, 6.8, 8.7 Hz, 1H), 1.92-1.53 (m, 7H), 1.51-1.38 (m, 2H).

Aufarbeitung

  1. customthe reaction temperature below 40° C
  2. temperaturethe reaction mixture was cooled to ice bath temperature
  3. extractionextracted with EtOAc
  4. additionby adding 50% NaOH solution
  5. extractionextracted with CHCl3
  6. washThe combined organic layer was washed with brine
  7. dry with materialdried over Na2SO4
  8. customthe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-5fb4344bbf1e4bc58428c68708c3e7ad
Quelldatensatz
uspto-grants-2011_07
Patentnummer
US07985759B2

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