Hydrochloric Acid → 4-Bromo-3-chloro-2-methylsulphenylbenzoic acid
Reaction equation
C([Li])CCC.C(NC(C)C)(C)C.[Br:13][C:14]1[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[CH:16][C:15]=1[Cl:23].[CH3:24][S:25]SC.Cl>O1CCCC1>[Br:13][C:14]1[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[C:16]([S:25][CH3:24])[C:15]=1[Cl:23]Participants
Procedure
n-Butyllithium (2.5M in hexane; 8.8 ml) was added to a stirred cooled solution of di-isopropylamine (2.22 g) in dry tetrahydrofuran, maintaining the temperature below -40° C. The mixture was stirred for 0.5 hours then a solution of 4-bromo-3-chlorobenzoic acid (2.36 g) in dry tetrahydrofuran was added. The mixture was stirred at -40° C. for 6 hours. Dimethyl disulphide (2.82 g) was added and the mixture was stirred at -40° C. for 1 hour and at room temperature overnight. Hydrochloric acid (2M) was added and the layers were separated. The organic layer was washed with water, dried (magnesium sulphate) and filtered. The filtrate was evaporated to dryness and the residue was recrystallized from a mixture of ethyl acetate and hexane to give 4-bromo-3-chloro-2-methylsulphenylbenzoic acid (0.98 g) as a solid, m.p. 128°-130° C.
Workup
- temperaturemaintaining the temperature below -40° C
- stirringThe mixture was stirred at -40° C. for 6 hours
- stirringthe mixture was stirred at -40° C. for 1 hour and at room temperature overnight
- customthe layers were separated
- washThe organic layer was washed with water
- dry with materialdried (magnesium sulphate)
- filtrationfiltered
- customThe filtrate was evaporated to dryness
- customthe residue was recrystallized from a mixture of ethyl acetate and hexane
Sources & evidence
- ORD record
- ord-01817be5a627479e8df0d680385beef9
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05804532
Reaction notes
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