Reaction equation
O[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][CH:3]=1.[Cl:12]C1C=C2C(C(=O)CCN2)=CC=1>>[Cl:12][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][CH:3]=1Participants
3
Procedure
a yield of 4-hydroxyquinoline of 15% relative to the 7-chloro-1,2,3,4-tetrahydroquinolin-4-one converted.
Sources & evidence
- ORD record
- ord-a8194d03635143faba0f7ef523855357
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04412076
Linked notes
Loading…