Potassium Carbonate → HCID 178518987, compound

HRID 2410318Notes

Reaction equation

HRID 2410318 reaction equation
S(O)(O)(=O)=O.[NH2:6]O.C(=O)([O-])[O-].[K+].[K+].S([O-])([O-])=O.[Na+].[Na+].[OH:20][C:21]1[CH:30]=[CH:29][CH:28]=[C:27]([O:31][CH2:32][C:33]([F:36])([F:35])[F:34])[C:22]=1[C:23](OC)=[O:24]>O>[F:34][C:33]([F:36])([F:35])[CH2:32][O:31][C:27]1[C:22]2[C:23]([OH:24])=[N:6][O:20][C:21]=2[CH:30]=[CH:29][CH:28]=1

Participants

6

Conditions

Temperature
50 °C

Procedure

To a solution of hydroxylamine sulfate (120 g, 732 mmol) in water (360 mL) was added potassium carbonate (121 g, 875 mmol) at 0° C. After 30 min of stirring, sodium sulfite (3.74 g, 29.7 mmol) and a methanolic solution of methyl 2-hydroxyl-6-(2,2,2-trifluoroethoxy)benzoate (36.4 g, 146 mmol, EXAMPLE 1, step 1, in 360 mL of methanol) were added to the mixture. Then the mixture was warmed to 50° C. and stirred for 30 h. After cooling to room temperature, reaction mixture was partially concentrated to approx. ⅔ volume and acidified with 2N hydrochloric acid. Product was extracted three times with ethyl acetate. Combined organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure to afford the desired product as a crystalline solid. Crude product (36.3 g) was used for the next step without further purification.

Workup

  1. stirringstirred for 30 h
  2. temperatureAfter cooling to room temperature
  3. customreaction mixture
  4. concentrationwas partially concentrated to approx. ⅔ volume
  5. extractionProduct was extracted three times with ethyl acetate
  6. washCombined organic layer was washed with brine
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-8a1353f93a184da689aaa79b054f5141
Source dataset
uspto-grants-2014_08
Patent number
US08816090B2

Reaction notes

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