Benzaldehyde → HCID 6453905, compound
Reaction equation
Cl.Cl.[CH3:3][O:4][C:5](=[O:12])[C@H:6]([CH2:8][CH2:9][CH2:10][NH2:11])[NH2:7].C(=O)C1C=CC=CC=1.C(OCC)C>C(Cl)Cl>[CH3:3][O:4][C:5](=[O:12])[C@H:6]([CH2:8][CH2:9][CH2:10][NH2:11])[NH2:7]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
Approximately 6.8 kg of ornithine methyl ester dihydrochloride is suspended in 10 l of methylene chloride, cooled to 0° C. and 6.5 kg of benzaldehyde, dissolved in 10 l of methylene chloride, is added at such a rate as to maintain the reaction temperature at 0° to -5° C. The reaction mixture is allowed to warm to room temperature, stirring continued for an additional 2 hours, and 20 l of diethyl ether added thereto. Upon standing overnight, the triethylammonium hydrochloride that precipitates is removed by filtration, and the precipitate is washed with an additional 6.8 liters of diethyl ether. The combined filtrates are evaporated in vacuo and the residue dissolved in 34 l of diethyl ether. The organic solution is washed four times with 4 l of water, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to yield 9.28 kg of dibenzaldimine ornithine methyl ester as an oil.
Workup
- additionis added at such a rate as
- temperatureto maintain the reaction temperature at 0° to -5° C
- temperatureto warm to room temperature
- waitUpon standing overnight
- customthe triethylammonium hydrochloride that precipitates
- customis removed by filtration
- washthe precipitate is washed with an additional 6.8 liters of diethyl ether
- customThe combined filtrates are evaporated in vacuo
- dissolutionthe residue dissolved in 34 l of diethyl ether
- washThe organic solution is washed four times with 4 l of water
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
- customevaporated in vacuo
Sources & evidence
- ORD record
- ord-11b6b654258243758a2e6e0159d5ef8d
- Source dataset
- uspto-grants-1982_05
- Patent number
- US04330559
Reaction notes
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