Boron tribromide → 85893-94-3
Reaction equation
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([O:9]C)[CH:5]=[CH:4][C:3]=1[C:11]1[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][C:14]=2[S:13][N:12]=1.B(Br)(Br)Br>ClCCCl>[S:13]1[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=2[C:11]([C:3]2[CH:4]=[CH:5][C:6]([OH:9])=[C:7]([Cl:8])[C:2]=2[Cl:1])=[N:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture containing 8.2 g of 3-(2,3-dichloro-4-methoxyphenyl)benzisothiazole, 100 ml of 1,2-dichloroethane and 100 ml of BBr3 was refluxed for 30 minutes. Itwas then poured into ice/water and the organic solvent was removed under reduced pressure. The product was then filtered off, washed with hexane and dried to give 7.50 g (96%) of 4-(benzisothiazol-3-yl)-2,3-dichlorophenol.
Workup
- temperaturewas refluxed for 30 minutes
- customthe organic solvent was removed under reduced pressure
- filtrationThe product was then filtered off
- washwashed with hexane
- customdried
Sources & evidence
- ORD record
- ord-5edaaa91988e4045af5b1a7b7af4ff01
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04868188
Reaction notes
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