4-(Trifluoromethyl)aniline → HCID 19901121, compound
Reaction equation
[S:1]1[CH2:4][S:3][C:2]1=[C:5]([C:12](C(OOCC)=O)=[O:13])[C:6]([O:8][CH:9]([CH3:11])[CH3:10])=[O:7].[NH2:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:23][CH:22]=1>>[S:3]1[CH2:4][S:1][C:2]1=[C:5]([C:12](=[O:13])[NH:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]([F:28])([F:29])[F:30])=[CH:23][CH:22]=1)[C:6]([O:8][CH:9]([CH3:10])[CH3:11])=[O:7]Participants
3
Procedure
Following the procedure of Example 18, the titled compound was prepared as a white solid (67%) from isopropyl 2-(1,3-dithietan-2-ylidene)-2-(ethoxycarboxycarbonyl)acetate and 4-aminobenzotrifluoride.
Sources & evidence
- ORD record
- ord-b7080c081f7b423a891622940e53fe36
- Source dataset
- uspto-grants-1992_04
- Patent number
- US05103013
Reaction notes
Loading…