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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 6-Amino-3-methyl-5-nitro-1,2-benzisothiazole | HCID 18314498 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-Chloro-3-methyl-5-nitro-1,2-benzisothiazole | HCID 18314481 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313295B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-31178e7d6a9c4c6e8871c081174f899a |
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| Source note | uspto-grants-2001_11 |
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