Potassium Carbonate → Methyl 4,5-Dibromo-1-Methylpyrrole-2-Carboxylate

HRID 1525532Notes

Reaction equation

HRID 1525532 reaction equation
ClC(Cl)(Cl)[C:3]([C:5]1[N:6]([CH3:12])[C:7]([Br:11])=[C:8]([Br:10])[CH:9]=1)=[O:4].[C:15](=O)([O-])[O-:16].[K+].[K+]>CO>[CH3:15][O:16][C:3]([C:5]1[N:6]([CH3:12])[C:7]([Br:11])=[C:8]([Br:10])[CH:9]=1)=[O:4]

Participants

4

Procedure

2,2,2-trichloro-1-(4,5-dibromo-1-methyl-1H-pyrrol-2-yl)-ethanone 14 (1.00 g, 2.60 mmol), anhydrous potassium carbonate (0.719 g, 5.20 mmol), and anhydrous methanol (20 mL) were charged into a reaction flask. The resulting suspension was stirred for 16 h at room temperature upon which the reaction was quenched with water (10 mL). The methanol was removed under reduced pressure and the residue partitioned between ethyl acetate (100 mL) and water (20 mL). The organic layer was subsequently washed with sat. NaHCO3 (2×30 mL), brine (2×20 mL), dried over anhydrous sodium sulfate, and filtered. Evaporation of the filtrate yielded the title compound (0.710 g, 92%) as a white solid: 1H NMR (300 MHz, DMSO-d6) δ 7.05 (s, 1H), 3.90 (s, 3H), 3.76 (s, 3H); 13C NMR (75 MHz, DMSO-d6) δ 159.38, 123.62, 118.51, 113.93, 98.06, 51.58, 35.78; HRMS (FAB) calcd for C7H7Br2NO2 (M+) 294.8844. found 294.8861.

Workup

  1. customwas quenched with water (10 mL)
  2. customThe methanol was removed under reduced pressure
  3. customthe residue partitioned between ethyl acetate (100 mL) and water (20 mL)
  4. washThe organic layer was subsequently washed with sat. NaHCO3 (2×30 mL), brine (2×20 mL)
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customEvaporation of the filtrate

Sources & evidence

ORD record
ord-aec46441ca0b4f7d9b5d7bd5b076cfaf
Source dataset
uspto-grants-2015_07
Patent number
US09084423B2

Reaction notes

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