Lithium naphthalenide → (1R*,2R*,5R*)-8-Benzyl-1-phenyl-8-azabicyclo[3.2.1]octan-2-ol

HRID 2088097

Reaktionsgleichung

Reaktionsgleichung von HRID 2088097
[C-]1C2C(=CC=CC=2)C=CC=1.[Li+].[CH2:12]([N:19]1[C@@H:24]2[C@H:25](S(C3C=CC=CC=3)(=O)=O)[CH2:26][C@@:20]1([C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)[C@H:21]([OH:36])[CH2:22][CH2:23]2)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C1COCC1>[CH2:12]([N:19]1[C@@H:24]2[CH2:25][CH2:26][C@@:20]1([C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)[C@H:21]([OH:36])[CH2:22][CH2:23]2)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

Komponenten

4

Versuchsvorschrift

Lithium naphthalenide (200 ml, 0.6M in teterahydrofuran) was added dropwise into a −78° C. solution of (1R*,2R*,5S*,6R*)-8-benzyl-1-phenyl-6-phenylsulphonyl-8-azabicyclo[3.2.1]octan-2-ol (Description 4; 25 g, 57.7 mmol) in THF (350 ml). The mixture was quenched by addition of saturated ammonium chloride and warmed to room temperature The reaction mixture was partitioned between ethyl acetate and saturated ammonium chloride. The organic layer was washed (×2) with water then dried (MgSO4), filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with 5, 15 and 40% ethyl acetate/iso-hexanes to yield the title compound (14.3 g, 84.6%).

Aufarbeitung

  1. customThe mixture was quenched by addition of saturated ammonium chloride
  2. customwas partitioned between ethyl acetate and saturated ammonium chloride
  3. washThe organic layer was washed (×2) with water
  4. dry with materialthen dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was chromatographed on silica gel eluting with 5, 15 and 40% ethyl acetate/iso-hexanes

Quellen und Nachweise

ORD-Eintrag
ord-161e92622f60454e9cc151d3e58bf2c2
Quelldatensatz
uspto-grants-2004_04
Patentnummer
US06727249B2

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