4-Aminocyclohexanecarboxylic acid → Methyl 4-aminocyclohexane-1-carboxylate--hydrogen chloride (1/1)
Reaction equation
[NH2:1][CH:2]1[CH2:7][CH2:6][CH:5]([C:8]([OH:10])=[O:9])[CH2:4][CH2:3]1.[ClH:11].[CH3:12]O>>[ClH:11].[NH2:1][CH:2]1[CH2:7][CH2:6][CH:5]([C:8]([O:10][CH3:12])=[O:9])[CH2:4][CH2:3]1Participants
3
Procedure
To 5.109 g (35.680 mM) of 4-aminocyclohexane-carboxylic acid was added 50 ml of 10% HCl/methanol and the mixture was refluxed overnight. The solvent was then distilled off under reduced pressure and the residue was crystallized from methanol-diethyl ether to provide the title compound.
Workup
- temperaturethe mixture was refluxed overnight
- distillationThe solvent was then distilled off under reduced pressure
- customthe residue was crystallized from methanol-diethyl ether
Sources & evidence
- ORD record
- ord-aeb2297a17b2433a91c3e467c9acd3bb
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06235731B1
Reaction notes
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