Boron tribromide → HCID 15578389, compound
Reaction equation
[Br:1][C:2]1[C:7](=[O:8])[CH:6]=[C:5]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[Cl:15])[O:4][C:3]=1[C:16]([O:18]CC)=[O:17].B(Br)(Br)Br>ClCCl>[Br:1][C:2]1[C:7](=[O:8])[CH:6]=[C:5]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[Cl:15])[O:4][C:3]=1[C:16]([OH:18])=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred solution of ethyl 3-bromo-6-(2-chlorophenyl)-4-oxo-4H-pyran-2-carboxylate (2.3 g) and boron tribromide (2.5 ml) in dichloromethane (25 ml) was heated under reflux for 4 hours. A tan solid precipitated out. Water (25 ml) was added to the cooled mixture and the yellow solid was filtered off. Recrystallisation from glacial acetic acid yielded the title product as off-white needles (mp 205°-207° C. with decomposition).
Workup
- temperatureunder reflux for 4 hours
- customA tan solid precipitated out
- additionWater (25 ml) was added to the cooled mixture
- filtrationthe yellow solid was filtered off
- customRecrystallisation from glacial acetic acid
Sources & evidence
- ORD record
- ord-f6f02eb7dd6947c696758755ad096e9a
- Source dataset
- uspto-grants-1981_12
- Patent number
- US04304728
Reaction notes
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