[CH2:1]([NH:7][CH2:8][CH2:9][CH:10]1[O:14][C:13]([CH3:16])([CH3:15])[C:12]([CH3:18])([CH3:17])[O:11]1)[CH2:2][CH2:3][CH:4]=[CH:5][CH3:6].C1C=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+].Cl[C:32](=[O:37])[CH:33]([Cl:36])[CH2:34][CH3:35]>O>[CH2:1]([N:7]([CH2:8][CH2:9][CH:10]1[O:11][C:12]([CH3:17])([CH3:18])[C:13]([CH3:16])([CH3:15])[O:14]1)[C:32](=[O:37])[CH:33]([Cl:36])[CH2:34][CH3:35])[CH2:2][CH2:3][CH:4]=[CH:5][CH3:6]N-Hex-4-enyl-N-(4,4,5,5-tetramethyl-1,3-dioxolan-2-ylethyl)-amine (10 grams), benzene (100 ml), water (100 ml) and sodium carbonate (8 grams) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is cooled to a temperature of 5° to 10° C. and α-chlorobutanoyl chloride (7 grams) is added dropwise with stirring. After the addition is completed stirring is continued until the reaction mixture reaches room temperature. After this time the organic phase is separated from the aqueous phase and is washed with water. The washed solution is then dried over anhydrous magnesium sulfate, filtered and stripped of solvent under reduced pressure to yield the desired product N-hex-4-enyl-N-(4,4,5,5-tetramethyl-1,3-dioxolan-2-ylethyl)-α-chlorobutanamide.
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