Water → HCID 15068914, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[C:6]([OH:8])=O.C(N1C=CN=C1)(N1C=CN=C1)=O.[CH3:24][C:25]1[CH:26]=[C:27]([CH2:31][CH2:32][NH2:33])[CH:28]=[CH:29][CH:30]=1.O>C1COCC1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[C:6]([NH:33][CH2:32][CH2:31][C:27]1[CH:28]=[CH:29][CH:30]=[C:25]([CH3:24])[CH:26]=1)=[O:8]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3-methoxybenzoic acid (5.2 g, 0.034 mol) and carbonyldimidazole (5.5 g, 0.034 mol) in THF (200 ml) was stirred in a flask protected from moisture. To this solution was added 4.6 g (0.034 mol) of 2-(3-methylphenyl)ethylamine in a small volume of THF. Stirring was continued for 1 h and then the reaction mixture was poured into 500 ml of water and extracted twice with 100 ml portions of methylene chloride. The methylene chloride solution was washed with 5% HCl, 10% Na2CO3, and water. Evaportion of this solution afforded the amide G1 (8.7 g, 94%) as a viscous oil.
Workup
- extractionextracted twice with 100 ml portions of methylene chloride
- washThe methylene chloride solution was washed with 5% HCl, 10% Na2CO3, and water
Sources & evidence
- ORD record
- ord-aaceeb1a52b944719f61a985058b183a
- Source dataset
- uspto-grants-1994_06
- Patent number
- USRE034630
Reaction notes
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