2-Methoxybenzoyl isocyanate → HCID 54216050, compound
Reaction equation
[NH:1]=[C:2]1[NH:6][C:5]([C:11]([F:14])([F:13])[F:12])([C:7]([F:10])([F:9])[F:8])[C:4](=[C:15]([F:20])[C:16]([F:19])([F:18])[F:17])[S:3]1.[CH3:21][O:22][C:23]1[CH:33]=[CH:32][CH:31]=[CH:30][C:24]=1[C:25]([N:27]=[C:28]=[O:29])=[O:26]>C1(C)C=CC=CC=1>[F:14][C:11]([F:12])([F:13])[C:5]1([C:7]([F:10])([F:9])[F:8])[C:4](=[C:15]([F:20])[C:16]([F:17])([F:18])[F:19])[S:3][C:2]([NH:1][C:28]([NH:27][C:25](=[O:26])[C:24]2[CH:30]=[CH:31][CH:32]=[CH:33][C:23]=2[O:22][CH3:21])=[O:29])=[N:6]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In toluene (10 ml) was dissolved 2-imino-4,4-bis(trifluoromethyl)-5-(tetrafluoroethylidene)-1,3-thiazolidine (1.0 g), and 2-methoxybenzoylisocyanate (0.4 g) which is a starting compound was added thereto and the mixture was stirred at room temperature for 3 hours.
Workup
- additionwas added
Sources & evidence
- ORD record
- ord-0e3682c5779b44fe8d1e516a068909f0
- Source dataset
- uspto-grants-1993_06
- Patent number
- US05221685
Reaction notes
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