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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259698Generated: October 28, 2026

Boron trifluoride etherate → HCID 178505387, compound

https://huagongshe.com/reaction/259698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTert-Butyl nitriteHCID 10906—
ReactantHCID 178508047HCID 178508047—
CatalystHydrochloric acid-ironHCID 86633186—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178505387HCID 178505387—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(2,2-Difluoro-1,3-benzodioxol-4-yl)-4-nitropyrazole obtained above in Example 17 is reduced to 4-amino-3-(2,2-difluoro-1,3-benzodioxol-4yl)pyrazole according to the method described by Vogel (Practical Organic Chemistry, Fourth Edition p. 660: Fe/HCl). 0.8 g (0.003 mol) of 4-amino-3-(2,2-difluoro-1,3-benzodioxol-4-yl)pyrazole in solution in 10 ml of anhydrous THF is treated at 0° C. with a solution of 10 ml of THF-containing 1 ml (0.0081 mol) of boron trifluoride etherate. 0.6 ml (0.005 mol) of tert-butyl nitrite in solution in 5 ml of THF are then added to the reaction mixture. Stirring is maintained for 1 hour at 0° C., the reaction mixture is then diluted with pentane and filtered on a sintered glass. After drying, a beige powder is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523280
Source datasetuspto-grants-1996_06
ORD IDord-2cfb3708275249c39d9eb634bd280fd7
Source noteuspto-grants-1996_06