tert-Butyl mercaptan → Methyl 3-[(tert-butylthio)diazenyl]-6-fluoro-2-methylbenzoate
Reaction equation
[NH2:1][C:2]1[C:3]([CH3:13])=[C:4]([C:9]([F:12])=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].[N:14]([O-])=O.[Na+].C([O-])(=O)C.[K+].[CH3:23][C:24]([SH:27])([CH3:26])[CH3:25]>Cl.O.C(O)C>[C:24]([S:27][N:14]=[N:1][C:2]1[C:3]([CH3:13])=[C:4]([C:9]([F:12])=[CH:10][CH:11]=1)[C:5]([O:7][CH3:8])=[O:6])([CH3:26])([CH3:25])[CH3:23]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
To a solution of methyl 3-amino-6-fluoro-2-methylbenzoate (12.0 g, 65.5 mmol) in hydrochloric acid (6 N, 200 mL) was added a solution of sodium nitrite (4.97 g, 72.1 mmol) in water (10 mL) at 0° C., and the mixture was stirred for 2 hr. An aqueous potassium acetate solution (30%) was added to the reaction solution at 0° C. to adjust the reaction solution to pH 4, and a solution of 2-methylpropane-2-thiol (8.12 mL, 72.1 mmol) in ethanol (10 mL) was added. The reaction solution was stirred at room temperature for 12 hr, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure to give the title compound (18.5 g, yield 99%) as a crudely purified product.
Workup
- stirringThe reaction solution was stirred at room temperature for 12 hr
- extractionthe mixture was extracted with ethyl acetate
- dry with materialThe extract was dried over anhydrous sodium sulfate
- customthe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-1cbf438207524dc98b6243840b6d4f17
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08110585B2
Reaction notes
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