HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871571Generated: November 1, 2026
Sulfuric Acid → 5-Amino-1-(6-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-5-yl)pyrazole
https://huagongshe.com/reaction/1871571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloroacrylonitrile | HCID 70198 | — |
| Reactant | 5-Chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-6-yl-hydrazine | HCID 54498518 | — |
| Catalyst | Ethylenediaminetetraacetic acid disodium salt | HCID 13020083 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Amino-1-(6-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-5-yl)pyrazole | HCID 18691510 | 37.2% |
Reaction Steps
To a solution wherein 5-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-6-yl-hydrazine (900 mg, 3.5 mmol) and disodium ethylenediaminetetraacetate (1 mg) are in methanol (6 ml), 2-chloroacrylonitrile (919 mg, 10.5 mmol) was added dropwise at 60° C., and under reflux for 8 hours, subsequently concentrated sulfuric acid (0.5 ml, 9.4 mmol) was added to the solution and was further heated under reflux for 6 hours. After the reaction solution was allowed to cool, anhydrous sodium carbonate (1.17 g, 10.5 mmol) was added to the reaction solution, stirred for 4 hours, and had the solvent distilled off under reduced pressure. Subsequently, water was added to the residue, the solution was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was subjected to silica gel column chromatography to give 400 mg of 5-amino-1-(6-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-5-yl)-pyrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06103750 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-261d8e7013874480ae61c3a4dc14c1e9 |
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| Source note | uspto-grants-2000_08 |
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