Ethylamine → HCID 86736906, compound
Reaction equation
[CH3:1][CH:2]([C:15]1([O:20][CH2:19]1)[C:16]([OH:18])=[S:17])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[CH2:21]([N:23](CC)CC)C.CC(OC(=S)C1OC1)CCCCCCCCCCCC.[CH2:48]([NH+:50](CC)CC)[CH3:49].ClC(OCC)=O.C(N)C>O1CCCC1>[CH3:21][NH:23][C:16](=[O:18])[C:15]1([CH:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH3:1])[O:20][CH2:19]1.[CH2:48]([NH:50][C:16](=[S:17])[C:15]1([CH:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH3:1])[O:20][CH2:19]1)[CH3:49]Participants
Reactant 5
Product 2
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a stirred solution of 0.3 g (0.001 mole) of 2-tetradecylthioglycidic acid in 10 ml of anhydrous tetrahydrofuran (THF) at 0° C. (ice water bath) is added 1.01 g (0.001 mole) of triethylamine in a small amount of THF. The mixture is stirred at 0° C. for about 30 minutes. To the thus-formed triethylammonium 2-tetradecylthioglycidate is added 0.108 g (0.001 mole) of ethyl chloroformate in a small amount of THF and the mixture is stirred at about 0° C. (ice water bath) for about 3 hours to prepare the corresponding mixed anhydride (a ppt. of Et3NHCl is observed). A stoichiometric excess of ethylamine in THF is then added and the mixture stirred at room temperature for 16 hours. The THF solvent is concentrated to approximately 1/4 volume, water is added and the mixture extracted with ether. After drying the ether extract (Na2SO4), the solvent is removed in vacuo giving the desired product, N-ethyl-2-tetradecylthioglycidamide, in good yield.
Workup
- customto prepare the
- stirringthe mixture stirred at room temperature for 16 hours
- concentrationThe THF solvent is concentrated to approximately 1/4 volume, water
- additionis added
- extractionthe mixture extracted with ether
- dry with materialAfter drying the ether
- extractionextract (Na2SO4)
- customthe solvent is removed in vacuo
Sources & evidence
- ORD record
- ord-da93d27756e44f8aa9a3864a1785be3a
- Source dataset
- uspto-grants-1983_01
- Patent number
- US04370343
Reaction notes
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