Hydrochloric Acid → 2,1,3-Benzoxadiazole-5-carboxylic acid

HRID 1776340Notes

Reaction equation

HRID 1776340 reaction equation
[N:1]1[O:2][N:3]=[C:4]2[CH:9]=[C:8]([C:10]([O:12]CC)=[O:11])[CH:7]=[CH:6][C:5]=12.[OH-].[Na+].Cl>CO>[N:1]1[O:2][N:3]=[C:4]2[CH:9]=[C:8]([C:10]([OH:12])=[O:11])[CH:7]=[CH:6][C:5]=12

Participants

5

Conditions

Temperature
40 °C

Procedure

To a room temperature, stirred solution of ethyl benzo[c][1,2,5]oxadiazole-5-carboxylate (0.7 g, 3.626 mmol) in MeOH (30 mL) was added 10% NaOH solution (6 mL) and the reaction mixture was then stirred at 40° C. for 3 h. The reaction mixture was then acidified to pH ˜2 with 2 N HCl and the aqueous layer was extracted with DCM (3×150 mL). The combined organic extracts were washed with water (100 mL) and brine (100 mL), dried over anhydrous Na2SO4, filtered, and evaporated under reduced pressure to afford benzo[c][1,2,5]oxadiazole-5-carboxylic acid (0.49 g, 82%) as a solid.

Workup

  1. extractionthe aqueous layer was extracted with DCM (3×150 mL)
  2. washThe combined organic extracts were washed with water (100 mL) and brine (100 mL)
  3. dry with materialdried over anhydrous Na2SO4
  4. filtrationfiltered
  5. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-ad5a5a04379444789a96716ce2c7dccd
Source dataset
uspto-grants-2016_02
Patent number
US09265767B2

Reaction notes

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