Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681269Generated: November 2, 2026

Benzisothiazole → 1,2-Benzisothiazole, 5-nitro-

https://huagongshe.com/reaction/1681269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzisothiazoleHCID 9225—
ReactantPotassium NitrateHCID 24434—
Reactant1,2-Benzisothiazole, 5-nitro-HCID 198410—
Reactant1,2-Benzisothiazole, 7-nitro-HCID 198656—
SolventSulfuric AcidHCID 1118—
Product1,2-Benzisothiazole, 5-nitro-HCID 198410—
Product1,2-Benzisothiazole, 7-nitro-HCID 198656—
ProductHCID 19387300HCID 19387300—

Reaction Conditions

Temperature-40 °C

Reaction Steps

P.2 4-Nitrobenzisothiazole, 5-nitrobenzisothiazole and 7-nitrobenzisothiazole 300 g of benzisothiazole are added, with cooling, to 750 ml of concentrated sulfuric acid, the solution is cooled to -40° C., and 227.5 g of potassium nitrate are added in portions, in such a manner that the temperature does not rise above room temperature. After standing at room temperature for 15 hours, the reaction mixture is poured onto ice and the solid portion is filtered off and dried. The product is chromatographed on silica gel with tetrahydrofuran:methylene chloride:hexane 5:10:85. After evaporation, there are isolated from the fractions 5.5% of the theorectical yield of 4-nitrobenzisothiazole, 56.5% of the theoretical yield of 5-nitrobenzisothiazole and 36.8% of the theoretical yield of 7-nitrobenzisothiazole (compounds 16, 11 and 1, Table).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169951
Source datasetuspto-grants-1992_12
ORD IDord-1159bcb776a149679a1797dd68b982ab
Source noteuspto-grants-1992_12