1-(Aminomethyl)cyclohexane-1-carboxylic acid → HCID 68118073, compound
Reaction equation
[NH2:1][CH2:2][C:3]1([C:9]([OH:11])=[O:10])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.[CH2:12](Cl)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]/[CH:20]=[CH:21]\[CH2:22]/[CH:23]=[CH:24]\[CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]>[OH-].[Na+]>[CH2:12]([NH:1][CH2:2][C:3]1([C:9]([OH:11])=[O:10])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19]/[CH:20]=[CH:21]\[CH2:22]/[CH:23]=[CH:24]\[CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5 grams of aminomethylcyclohexanecarboxylic acid were dissolved in 50 cm3 of 6% sodium hydroxide. This solution was stirred vigorously and maintained at 10° C while 10 grams of linoleyl chloride were added drop by drop. The stirring was maintained for 1 hour at ambient temperature. The precipitate obtained on centrifuging was washed twice with acetone and allowed to dry.