Boron tribromide → HCID 10247007, compound
Reaction equation
[C:1]1([C:7]2[O:8][C:9]3[C:14]([C:15](=[O:23])[C:16]=2[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:13]([O:24]C)[C:12]([O:26]C)=[C:11]([O:28]C)[CH:10]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.B(Br)(Br)Br>C(Cl)Cl>[C:1]1([C:7]2[O:8][C:9]3[C:14]([C:15](=[O:23])[C:16]=2[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[C:13]([OH:24])[C:12]([OH:26])=[C:11]([OH:28])[CH:10]=3)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Similar to the preparation of 1d, the reaction of 2,3-diphenyl-5,6,7-trimethoxychromone with boron tribromide in methylene chloride at ° C. for 30 min and then at room temperature for 3 hr produces the title compound.
Sources & evidence
- ORD record
- ord-20266b789249489586d13372a35d75d7
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08138165B2
Reaction notes
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