Thionyl Chloride → 2-Bromophenylacetyl chloride
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=O.S(Cl)([Cl:14])=O>C1C=CC=CC=1>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([Cl:14])=[O:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
For 3 hours, 21 g (0.098 mole) of o-bromophenylacetic acid was refluxed in 100 ml of anhydrous benzene and 23.5 g (0.198 mole) of thionyl chloride. After completion of the reaction, benzene and unreacted thionyl chloride were removed by distillation under reduced pressure so that unreacted thionyl chloride was removed as completely as possible.
Workup
- customwere removed by distillation under reduced pressure so that unreacted thionyl chloride
- customwas removed as completely as possible
Sources & evidence
- ORD record
- ord-e032945e75a74b5995973d270c9a0711
- Source dataset
- uspto-grants-1981_08
- Patent number
- US04283532
Reaction notes
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