Water → (1S,3R,4R,6R)-4-Bromo-3,7,7-trimethylbicyclo[4.1.0]heptan-3-ol

HRID 2353588Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2353588
[CH:1]12[C:7]([CH3:9])([CH3:8])[CH:6]1[CH2:5][CH:4]=[C:3]([CH3:10])[CH2:2]2.C([O-])([O-])=O.[Ca+2].[Br:16]N1C(=O)CCC1=O.[OH2:24]>O1CCOCC1>[Br:16][C@@H:4]1[CH2:5][C@@H:6]2[C@@H:1]([C:7]2([CH3:9])[CH3:8])[CH2:2][C@@:3]1([CH3:10])[OH:24]

Komponenten

6

Versuchsvorschrift

To a suspension of (+)-3-carene (82 g, 0.6 mol) and CaCO3 (80 g, 0.8 mol) in water (300 mL) and dioxane (600 mL) is added N-bromosuccinimide (142 g, 0.8 mol). The mixture is stirred at rt for 1 h, diluted with water (1500 mL) and extracted with diethyl ether (500 mL). The organic extract is washed with water (3×1000 mL) and 5% aq. Na2S2O3 (2×500 mL), and dried over Na2SO4. The solvent is removed under reduced pressure and the crude product is purified by column chromatography on silica gel eluting with hexane/EA 4:1 to yield (1S,3R,4R,6R)-4-bromo-3,7,7-trimethyl-bicyclo[4.1.0]heptan-3-ol (48.3 g) as a beige solid. 1H NMR (CDCl3): δ 4.05 (dd, J=7.6, 10.6 Hz, 1H), 2.48-2.36 (m, 2H), 2.20 (dd, J=10.0, 14.7 Hz, 1H), 1.42-1.38 (m, 1H), 1.36 (s, 3H), 1.02 (s, 3H), 0.98 (s, 3H), 0.90-0.80 (m, 1H), 0.72-0.66 (m, 1H).

Aufarbeitung

  1. extractionextracted with diethyl ether (500 mL)
  2. extractionThe organic extract
  3. washis washed with water (3×1000 mL) and 5% aq. Na2S2O3 (2×500 mL)
  4. dry with materialdried over Na2SO4
  5. customThe solvent is removed under reduced pressure
  6. customthe crude product is purified by column chromatography on silica gel eluting with hexane/EA 4:1

Quellen und Nachweise

ORD-Eintrag
ord-fa6535d0463343269a059b66563e9fd2
Quelldatensatz
uspto-grants-2010_07
Patentnummer
US07750040B2

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