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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615355Generated: October 30, 2026

Sodium Hydroxide → 2-BENZOTHIAZOLESULFONAMIDE, 6-NITRO-

https://huagongshe.com/reaction/615355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium HydroxideHCID 14923—
ReactantPotassium PermanganateHCID 516875—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 178418579HCID 178418579—
SolventWaterHCID 962—
Product2-BENZOTHIAZOLESULFONAMIDE, 6-NITRO-HCID 13393427—

Reaction Conditions

Temperature25 °C

Reaction Steps

To ammonium hydroxide (14.8M) (90 ml.) were added dropwise simultaneously sodium hypochlorite solution (5.25%) (42.4 ml.) and a solution of sodium hydroxide (1.2 g., 0.03 mole) and 2-mercapto-6-nitrobenzothiazole (6.37 g., 0.03 mole) in H2O (80 ml.) with stirring at <5° C. After 1/2 hr. the precipitated solid was collected by suction filtration and washed well with ice-H2O. The wet solid was suspended in acetone (120 ml.) with stirring at 25° C., treated with glacial acetic acid (2.4 ml.), then immediately treated dropwise wth 5% aqueous potassium permanganate solution (6.6 g, 0.04 mole in 120 ml H2O) over a 1/2 hr. period maintaining the reaction mixture temperature at <30° C. After stirring for an additional hour, the mixture was filtered to remove precipitated manganese dioxide, and the filtrate concentrated to remove the acetone and precipitate the solid product. Crystallization from 1,2-dichloroethane gave 1.18 g 6-nitro-2-benzothiazolesulfonamide, m.p. 176°-178° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04499103
Source datasetuspto-grants-1985_02
ORD IDord-5aa57f890ba6420faa539552c3755d5e
Source noteuspto-grants-1985_02