stearic N-chloramide → HCID 54390578, compound
Reaction equation
Cl[NH:2][C:3](=[O:21])[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][CH2:17][CH2:18][CH2:19][CH3:20].[NH:22]([CH2:24][C:25](O)=O)[CH3:23].[OH-:28].[Na+]>O>[CH2:24]([NH:22][C:23]([NH:2][C:3](=[O:21])[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][CH2:17][CH2:18][CH2:19][CH3:20])=[O:28])[CH2:25][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In accordance with the procedures described in Example 19, 31.75 g (0.1 mol) stearic N-chloramide was reacted with sarcosine/sodium hydroxide in water to yield 88% by weight of N-n-heptadecyl-N'-stearoyl urea of the formula ##STR20## having a melting point of 110° C.
Sources & evidence
- ORD record
- ord-b1433ec7851241a3951bdf44c83d87a2
- Source dataset
- uspto-grants-1982_08
- Patent number
- US04346233
Reaction notes
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