Hydrochloric Acid → HCID 18477217, compound
Reaction equation
C1(=O)[N:5]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][C:25]([O:27]C)=[O:26])C(=O)C2=CC=CC=C12.O.NN.Cl>C(O)C>[NH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][C:25]([OH:27])=[O:26]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of methyl 20-phthalimidoeicosanoate (5.0 g, 10.6 mmoles), 100 ml of ethanol, 80% hydrazine hydrate (1.0 ml, 15.9 mmoles) was refluxed for 9 hours. After the addition of 26.5 ml of 6N aqueous hydrochloric acid, the reaction mixture was further refluxed for 1 hour. The insoluble matter that formed was removed by filtration. The filtrate was concentrated under reduced pressure. To the residue were added 70 ml of ethanol and 42.4 ml of 1N aqueous sodium hydroxide solution, and the obtained reaction mixture was refluxed for 16 hours. The reaction mixture was neutralized by adding 6N aqueous hydrochloric acid solution under ice-cooled condition. The precipitates that formed were collected by filtration and recrystallized from ethanolacetic acid-water, to give 20-aminoeicosanoic acid (2.50 g, 72%) having the following properties.
Workup
- temperaturewas refluxed for 9 hours
- temperaturethe reaction mixture was further refluxed for 1 hour
- customThe insoluble matter that formed
- customwas removed by filtration
- concentrationThe filtrate was concentrated under reduced pressure
- additionTo the residue were added 70 ml of ethanol and 42.4 ml of 1N aqueous sodium hydroxide solution
- customthe obtained reaction mixture
- temperaturewas refluxed for 16 hours
- temperaturecooled condition
- customThe precipitates
- customthat formed
- filtrationwere collected by filtration
- customrecrystallized from ethanolacetic acid-water
Sources & evidence
- ORD record
- ord-dfd6c2079b8944749242f4632abca4ad
- Source dataset
- uspto-grants-1993_08
- Patent number
- US05238837
Reaction notes
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