ethyl 4-(cyclopropylamino)cyclohexanecarboxylate synthesis

Yield:1083048-96-7 5.62 g

Reaction Conditions:

with sodium tris(acetoxy)borohydride;acetic acid in 1,2-dichloro-ethane at 20; for 14 h;

Steps:

9 Preparation Example 9

Preparation Example 9
To a mixture of 3.35 g of cyclopropylamine, 1.0 mL of acetic acid, 9.34 g of sodium triacetoxyborohydride, and 30 mL of 1,2-dichloroethane was added dropwise 5.00 g of ethyl 4-oxocyclohexane carboxylate at room temperature.
After stirring at room temperature for 14 hours, to the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution to quench the reaction.
To the reaction mixture was added chloroform, followed by extraction and then the organic layer was dried over anhydrous sodium sulfate.
After filtration, the solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (aqueous ammonia-methanol-chloroform) to obtain 5.62 g of ethyl 4-(cyclopropylamine)cyclohexane carboxylate as a colorless oily substance.

References:

EP2565190,2013,A1 Location in patent:Paragraph 0110