Hydrochloric Acid → 1H,3H-2,1,3-Benzothiadiazole 2,2-dioxide

HRID 2374597Notes

Reaction equation

HRID 2374597 reaction equation
[C:1]1([NH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH2:7].[S:9](N)(N)(=[O:11])=[O:10].O.Cl>COCCOCCOC>[NH:7]1[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[NH:8][S:9]1(=[O:11])=[O:10]

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 7243O-PhenylenediamineHCID 82267Sulfamide

Product 1

HCID 153721H,3H-2,1,3-Benzothiadiazole 2,2-dioxideYield 45.1%

Reagents, catalysts & solvents 1

HCID 8150DiglymeSolvent

Procedure

A solution of orthophenylenediamine (20 g) and sulfamide (20.4 g) in diglyme (200 ml) was stirred at 160° C. for 2 hours, the reaction mixture was cooled to room temperature, water (200 g) was poured thereto, hydrochloric acid was added until pH 1, extracted with ethyl acetate, and washed with 1N hydrochloric acid. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give a reddish brown solid (14.2 g). Further recrystallization from ethanol-diethyl ether afforded the title compound as colorless crystals (13.2 g).

Workup

  1. extractionextracted with ethyl acetate
  2. washwashed with 1N hydrochloric acid
  3. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-4d273bebb4ee40638e7658ac7754dbef
Source dataset
uspto-grants-2008_12
Patent number
US07462628B2

Reaction notes

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