Glycol monoethyl ether → HCID 20525890, compound
Reaction equation
Cl.[CH2:2]([NH:18][C:19]1[CH:29]=[CH:28][C:22]([CH2:23][CH2:24][C:25](Cl)=[O:26])=[CH:21][CH:20]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[CH2:30]([O:32][CH2:33][CH2:34][OH:35])[CH3:31]>CN(C)C1C=CN=CC=1.C(Cl)Cl>[CH2:2]([NH:18][C:19]1[CH:29]=[CH:28][C:22]([CH2:23][CH2:24][C:25]([O:35][CH2:34][CH2:33][O:32][CH2:30][CH3:31])=[O:26])=[CH:21][CH:20]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Prepared as described in Example 18, 10.0 g. of 4-(hexadecylamino)hydrocinnamoyl chloride hydrochloride in 80. ml. of methylene chloride is treated with 9.5 g. of 4-dimethylaminopyridine and 2.1 g. of 2-ethoxyethanol, analogous to the method of Example 19. Workup and filtration through alumina provides 2-ethoxyethyl 4-(hexadecylamino)hydrocinnamate.
Workup
- customPrepared
- filtrationWorkup and filtration through alumina
Sources & evidence
- ORD record
- ord-db7b1ffb1f6b48ac9fceb73b5cb13496
- Source dataset
- uspto-grants-1982_09
- Patent number
- US04348399
Reaction notes
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