Reaction equation
[NH2:1][CH2:2][C:3]([OH:5])=O.[OH-].[Na+].[CH2:8]([O: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]CC)[CH:9]1[O:11][CH2:10]1.Cl.[CH2:28](O)[CH3:29]>>[OH:5][CH2:3][CH2:2][NH:1][CH2:28][CH2:29][C:9]([CH3:10])([OH:11])[CH2:8][O:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]Participants
6
Conditions
- Temperature
- 80 °C
Procedure
A 300-ml two-necked flask equipped with a stirrer was charged with 7.51 g (0.1 mol) of glycine, 8.3 g (0.1 mol) of 48% NaOH and 200 ml of ethanol. While stirring the mixture at 80° C., an ethanol solution of 2.70 g (10 mmol) of tetradecyl glycidyl ether was added, and the resultant mixture was stirred for 3 hours. After ethanol was distilled off under reduced pressure, methanol and hydrochloric acid was added to the mixture to acidify it. The mixture was subjected to extraction with chloroform. The resultant extract was concentrated under reduced pressure, and the residue was then purified by column chromatography on silica gel, thereby obtaining 1.17 g (yield: 30.7%) of the title compound [(IIa-10) hydrochloride].
Workup
- customA 300-ml two-necked flask equipped with a stirrer
- distillationAfter ethanol was distilled off under reduced pressure, methanol and hydrochloric acid
- additionwas added to the mixture
- extractionThe mixture was subjected to extraction with chloroform
- extractionThe resultant extract
- concentrationwas concentrated under reduced pressure
- customthe residue was then purified by column chromatography on silica gel
Sources & evidence
- ORD record
- ord-5d521726c64849569940c6f7bb84cf4f
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05723497
Linked notes
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