Ethanolamine → HCID 20278973, compound
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11](=[O:16])[C:12]([Cl:15])([Cl:14])[Cl:13])(=O)[CH3:2].[NH2:17][CH2:18][CH2:19][OH:20]>C(O)C>[Cl:13][C:12]([Cl:15])([Cl:14])[C:11]([NH:10][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[C:1](=[N:17][CH2:18][CH2:19][OH:20])[CH3:2])=[O:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 60 parts of N-(2-acetylphenyl)-2,2,2-trichloroacetamide, 14 parts of 2-aminoethanol and 200 parts of ethanol is stirred first for 5.50 hours at reflux and further overnight while the temperature is allowed to cool to room temperature. The formed precipitate is filtered off. The product is washed with 2,2'-oxybispropane and dried in vacuo, yielding 40 parts (59%) of 2,2,2-trichloro-N-[2-[1-[(2-hydroxyethyl)imino]ethyl]phenyl]acetamide; mp. 182° C.
Workup
- temperatureat reflux and further overnight while the temperature
- filtrationThe formed precipitate is filtered off
- washThe product is washed with 2,2'-oxybispropane
- customdried in vacuo
Sources & evidence
- ORD record
- ord-d864191d968845c6997f4cc5b2fc93f2
- Source dataset
- uspto-grants-1982_06
- Patent number
- US04335127
Reaction notes
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