Thionyl Chloride → 3-Bromofuran-2-carbonyl chloride
Reaction equation
[Br:1][C:2]1[CH:6]=[CH:5][O:4][C:3]=1[C:7]([OH:9])=O.S(Cl)([Cl:12])=O>>[Br:1][C:2]1[CH:6]=[CH:5][O:4][C:3]=1[C:7]([Cl:12])=[O:9]Participants
3
Procedure
Compounds of this invention with Formulae I-IX may be prepared as illustrated by the exemplary reaction in Scheme 2. Reaction of 3-bromo-furan-2-carboxylic acid with thionyl chloride produces intermediate, 3-bromo-furan-2-carbonyl chloride, followed by refluxing with 4-trifluoromethyl-benzamidoxime in pyridine produces the product 5-(3-bromo-furan)-3-(4-trifluoromethyl-phenyl)-[1,2,4]-oxadiazole.
Workup
- customCompounds of this invention with Formulae I-IX may be prepared
- customas illustrated by the exemplary reaction in Scheme 2
Sources & evidence
- ORD record
- ord-209a46d3a39a4c428b257bbcc119fb2d
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07435750B2
Reaction notes
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