HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369601Generated: October 29, 2026
Dichloromethane → 6-Fluoro-3-methyl-5-nitro-1,2-benzisothiazole
https://huagongshe.com/reaction/369601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 6-Chloro-3-methyl-5-nitro-1,2-benzisothiazole | HCID 18314481 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Fluoro-3-methyl-5-nitro-1,2-benzisothiazole | HCID 18314469 | — |
Reaction Steps
A mixture of 6-chloro-3-methyl-5-nitro-1,2-benzisothiazole (2.25 g, 9.80 mmol), potassium fluoride (2.85 g, 49.0 mmol), and 18-crown-6 (1.50 g, 5.70 mmol) in acetonitrile is heated in a sealed tube for 29 days, filtered to remove solids, and partially concentrated in vacuo to obtain a liquid. The liquid is diluted with ethyl acetate, washed sequentially with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a dark, brown solid. Flash column chromatography of the solid using silica gel and a 10% to 50% ethyl acetate in hexanes gradient gives a yellow solid containing two components. Flash column chromatography of the yellow solid using silica gel and a 50% to 70% methylene chloride in hexanes gradient gives the title product as a pale, yellow solid (0.870 g, mp 118-119° C.) which is identified by NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140270 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-2b007e66851b4d209ac20a77513a4095 |
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| Source note | uspto-grants-2000_10 |
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