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ChemicalBook CAS DataBase List Teprenone

Teprenone synthesis

9synthesis methods
-

Yield:6809-52-5 50%

Reaction Conditions:

with potassium hydroxide in methanol;water at 80 - 85; for 2 h;

Steps:

1 5E,9E,13E-Geranylgeranyl acetone 12 (5-trans-GGA)
A mixture of 3-rac-ketoester 11, (0.07 g, 0.174 mmol) MeOH (0.3 mL), and 5N aqueous KOH (0.15 mL) was heated at 80-85° C. for 2 h, reaction was followed by TLC.
After cooling the reaction mixture, it was acidified with 2N HCl and extracted with diethyl ether, ethyl acetate or hexanes (3*400 mL).
The combined organic layers were successively washed with water, aqueous NaHCO3, brine and dried over anhydrous MgSO4.
After removal of solvent, the oily crude product was purified by silica gel column chromatography using n-hexanes to 1-2% EtOAc in n-Hexanes to afford a colorless liquid of 5-trans-GGA 12. Yield: 0.028 g (50%). TLC Rf: 0.45 (5% EtOAc/n-hexanes); LCMS: MS (m/z): 333 (MH+); 353 (M+Na).

References:

Coyote Pharmaceuticals, Inc.;Serizawa, Hiroaki;Argade, Ankush B.;Datwani, Akash;Spencer, Natalie US2013/85283, 2013, A1 Location in patent:Paragraph 0180

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