[CH:1](NC(C)C)(C)C.C([Li])CCC.[CH:13]1([C:19]([OH:21])=[O:20])[CH2:18][CH2:17][CH:16]=[CH:15][CH2:14]1.IC>C1COCC1>[CH3:1][C:13]1([C:19]([OH:21])=[O:20])[CH2:18][CH2:17][CH:16]=[CH:15][CH2:14]1N-isopropylpropan-2-amine (50.1 g, 69.5 mL, 495.5 mmol) was dissolved in 50 mL of THF. To the solution was added n-butyllithium (174.4 mL of 2.5 M solution in hexanes, 436.0 mmol) at −78° C. The resulting solution was stirred for 30 minutes at −78° C. To the reaction was then added cyclohex-3-ene-1-carboxylic acid (25.0 g, 198.2 mmol) and the reaction was allowed to warm to 60° C. for 2 hrs. The reaction was cooled to room temp and iodomethane (29.5 g, 13.0 mL, 208.1 mmol) was added and the reaction was allowed to stir overnight and then quenched with 1 N HCl until the pH<4. The crude product was extracted into CH2Cl2 and water. The organic phase was concentrated in vacuo to a yellow oil (27 g) and used without further purification.
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