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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428397Generated: October 28, 2026

Hydrochloric Acid → 6-Chloro-3-methyl-5-nitro-1,2-benzisothiazole

https://huagongshe.com/reaction/428397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-Butyl nitriteHCID 10906—
Reactant6-Amino-3-methyl-5-nitro-1,2-benzisothiazoleHCID 18314498—
CatalystCupric ChlorideHCID 24014—
SolventAcetonitrileHCID 6342—
Product6-Chloro-3-methyl-5-nitro-1,2-benzisothiazoleHCID 18314481—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of tert-butyl nitrite (3.30 mL, 0.0278 mol) and copper(II) chloride (2.98 g, 0.0222 mol) in acetonitrile is heated to 65° C., treated portionwise with 6-amino-3-methyl-5-nitro-1,2-benzisothiazole (3.88 g, 0.0185 mol), stirred at 65° C., cooled to room temperature, and poured into 20% hydrochloric acid. The resultant aqueous mixture is extracted with ethyl acetate. The organic extracts are combined, washed with 20% hydrochloric acid, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a solid. Flash column chromatography of the solid using silica gel and methylene chloride/hexanes solutions (1:1 and 3:1) gives the title product as a pale, yellow solid (2.54 g, mp 156-158° C.) which is identified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313295B1
Source datasetuspto-grants-2001_11
ORD IDord-31178e7d6a9c4c6e8871c081174f899a
Source noteuspto-grants-2001_11