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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871568Generated: October 26, 2026

Sulfuric Acid → 5-Amino-1-(6-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-5-yl)-3-cyanopyrazole

https://huagongshe.com/reaction/1871568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantNitrosylsulfuric acidHCID 82157—
ReactantSodium AcetateHCID 517045—
ReactantEthyl 2,3-DicyanopropionateHCID 10725530—
Reactant6-Amino-5-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuranHCID 15477347—
ReactantMethyl 2,3-dicyanopropanoateHCID 15477348—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-Amino-1-(6-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-5-yl)-3-cyanopyrazoleHCID 15477349—

Reaction Steps

To a solution wherein 6-amino-5-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran (2.41 g, 10.0 mmol) is in acetic acid (30 ml), a nitrosylsulfuric acid solution prepared from sodium nitrite (760 mg, 11.0 mmol) and concentrated sulfuric acid (5.5 ml) was added dropwise at 10 to 15° C. over a period of about 10 minutes. The reaction solution was added dropwise to a mixture consisting of sodium acetate (7 g) and a 1:1 mixture (1.45 g) of methyl 2,3-dicyanopropionate and ethyl 2,3-dicyanopropionate, and 50 ml of water under vigorous stirring at room temperature and further stirred for 30 minutes. After reaction solution was extracted with chloroform, the organic layer was washed with a saturated sodium hydrogencarbonate solution, then dried over anhydrous magnesium sulfate and concentrated under reduced pressure until the amount of the solution became about 20 ml. 5 ml of ammonia water was added to the resulting solution and stirred at room temperature for 2 hours. After water was poured into the solution, the solution was extracted with chloroform, the organic layer was washed with a 1N hydrochloric acid solution and then 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 1.0 g of 5-amino-1-(6-chloro-1,1,3,3-tetrafluoro-1,3-dihydroisobenzofuran-5-yl)-3-cyanopyrazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06103750
Source datasetuspto-grants-2000_08
ORD IDord-5a8bf6c2fd5448438cca8b13a548d4ca
Source noteuspto-grants-2000_08