Reaction equation
[Br:1][C:2]1[C:3]([F:13])=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9]C(=O)[C:7]2=[O:12].[OH-:14].[Na+].OO.Cl>O>[NH2:9][C:10]1[C:2]([Br:1])=[C:3]([F:13])[CH:4]=[CH:5][C:6]=1[C:7]([OH:12])=[O:14]Participants
Conditions
- Temperature
- 45 °C
Procedure
A 2 L 3-neck flask with a temperature probe adapter was fixed with a mechanical stirrer, addition funnel, and temperature probe. The flask was charged with 7-bromo-6-fluoroindoline-2,3-dione (719b; 11.53 g, 47.3 mmol) and 1 N NaOH (104 mL, 104 mmol) at RT; 30% hydrogen peroxide (10.62 mL, 104 mmol) was added via addition funnel over 15 min when the temperature of the brown solution raised to 45° C. The reaction mixture was stirred for 1.5 h when mostly product was observed via LCMS. The slurry was acidified to pH 7 with 2 N HCl when a solid was still present; the reaction mixture was diluted with water (100 mL) to effect stirring when it began to bubble. The slurry was then acidified to pH 1.8 with 2 N HCl (no exotherm was observed). After stirring at RT for 30 min, the slurry was filtered, washed with water, and dried in a vacuum oven to give 2-amino-3-bromo-4-fluorobenzoic acid (9.90 g, 42.3 mmol, 90% yield) as a beige solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 6.59 (t, J=8.61 Hz, 1H) 7.08 (br. s., 2H) 7.86 (dd, J=8.90, 6.75 Hz, 1H) 13.04 (br. s., 1H). 19F NMR (377 MHz, DMSO-d6) δ ppm −97.39 (s, 1F). MS (ESI, pos. ion) m/z: 233.9/235.9 (M+1).
Workup
- additionA 2 L 3-neck flask with a temperature probe adapter was fixed with a mechanical stirrer, addition funnel
- stirringto effect stirring when it
- customto bubble
- stirringAfter stirring at RT for 30 min
- filtrationthe slurry was filtered
- washwashed with water
- customdried in a vacuum oven
Sources & evidence
- ORD record
- ord-125aebd2593b4ca1a2fd3c500f952f70
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09394297B2
Linked notes
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