Hydrochloric Acid → HCID 19752110, compound
Reaction equation
C([NH:4][C:5]1([CH2:13][NH:14]C(=O)C)[CH2:10][CH:9]2[CH2:11][CH2:12][CH:6]1[CH2:7][CH2:8]2)(=O)C.[ClH:18]>O>[ClH:18].[ClH:18].[NH2:4][C:5]1([CH2:13][NH2:14])[CH2:10][CH:9]2[CH2:11][CH2:12][CH:6]1[CH2:7][CH2:8]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The procedure is as Example 1, but starting from 2-acetylamino 2-acetylaminomethyl-bicyclo[2.2.2]octane (4.6 g) in a 6N solution (100 cc) of hydrochloric acid in water for 48 hours under reflux; taking up the residue from the evaporation in ethanol (25 cc) and diethyl ether (75 cc), 2-amino-2-aminomethyl-bicyclo[2.2.2]octane dihydrochloride (3 g) is obtained in the form of white crystals which melt at 302°-303° C.
Workup
- temperatureunder reflux
- customfrom the evaporation in ethanol (25 cc)
Sources & evidence
- ORD record
- ord-86a81c5f81af4fc0b3102e70d3c3e290
- Source dataset
- uspto-grants-1993_07
- Patent number
- US05225207
Reaction notes
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