Ammonia → 2,1,3-benzoxadiazole-4-sulfonamide

HRID 1252852Notes

Reaction equation

HRID 1252852 reaction equation
[N:1]1[O:2][N:3]=[C:4]2[C:9]([S:10](Cl)(=[O:12])=[O:11])=[CH:8][CH:7]=[CH:6][C:5]=12.O1CCCC1.[NH3:19].[OH-].[NH4+]>O>[N:1]1[O:2][N:3]=[C:4]2[C:9]([S:10]([NH2:19])(=[O:12])=[O:11])=[CH:8][CH:7]=[CH:6][C:5]=12

Participants

6

Reactant 4

HCID 222AmmoniaHCID 8028TetrahydrofuranHCID 14923Ammonium HydroxideHCID 27354462,1,3-Benzoxadiazole-4-sulfonyl chloride

Product 1

HCID 27565902,1,3-benzoxadiazole-4-sulfonamide

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a stirred solution of 3.0 g of 2,1,3-benzoxadiazole-4-sulfonyl chloride and 200 mL of tetrahydrofuran at -30° C. was added 10 mL of ammonia under an inert atmosphere. The resulting suspension was stirred at ambient temperature for 3 hours. Concentrated ammonium hydroxide (20 mL) and water (20 mL) were added. The reaction was extracted with ethyl acetate and the organic extracts were combined, dried over magnesium sulfate, filtered, and stripped to give a crude solid. Recrystallization from chlorobutanethanol afforded 1.82 g of the title compound as an orange-tan solid, m.p. 157°-159° C.

Workup

  1. extractionThe reaction was extracted with ethyl acetate
  2. dry with materialdried over magnesium sulfate
  3. filtrationfiltered
  4. customto give a crude solid
  5. customRecrystallization from chlorobutanethanol

Sources & evidence

ORD record
ord-62e6e68850bb4cd98bf4ce73b9462706
Source dataset
uspto-grants-1988_05
Patent number
US04746356

Reaction notes

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