Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:9]([OH:11])=[O:10])=[N:6][C:7]=1Cl.[OH-].[K+].[F:14][C:15]([F:20])([F:19])[CH:16]([OH:18])[CH3:17].Cl>CS(C)=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:9]([OH:11])=[O:10])=[N:6][C:7]=1[O:18][CH:16]([CH3:17])[C:15]([F:20])([F:19])[F:14]Participants
6
Procedure
5-Bromo-6-chloropicolinic acid (5 g, 21.1 mmol; CAN 959958-25-9) was dissolved in DMSO (100 mL) to give a colorless solution. To this solution potassium hydroxide (4.75 g, 84.6 mmol) was added. The reaction mixture turned into a white suspension which was stirred for 15 min. Then 1,1,1-trifluoropropan-2-ol (2.41 g, 1.92 mL, 21.1 mmol) was added. The mixture was stirred for 1 d at ambient temp., poured onto icewater/1N HCl (200 mL) and extracted with EtOAc (2×400 mL). The organic layers were washed with icewater/brine (200 mL), combined and dried over Na2SO4 and concentrated in vacuo to give the title compound (6.9 g, quant.) as orange solid. MS (EI): m/e=312.3 [M−H]−.
Workup
- customto give a colorless solution
- stirringThe mixture was stirred for 1 d at ambient temp.
- extractionextracted with EtOAc (2×400 mL)
- washThe organic layers were washed with icewater/brine (200 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-1c01380cd22a41c18868a60340162e3c
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290451B2
Linked notes
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