Hydrochloric Acid → Methyl 6-aminohexanoate hydrochloride
Reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8].[ClH:11]>O1CCOCC1>[ClH:11].[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([O:9][CH3:10])=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The methyl 6-aminohexanoate was dissolved in 40 mL of dioxane, followed by addition of 7.1 mL of 4N-hydrochloride solution of dioxane. After the mixture was stirred at room temperature for 30 minutes, the solvent was distilled off, followed by addition of ether to the residue. The precipitated crystals were isolated by filtration and dried under reduced pressure to yield 3.3 g of the target compound.
Workup
- distillationthe solvent was distilled off
- additionfollowed by addition of ether to the residue
- customThe precipitated crystals were isolated by filtration
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-bf5d63434cea466ebc6e34773baa4bef
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07202093B2
Reaction notes
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