HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634562Generated: October 30, 2026
Nitric Acid → 1-Methyl-5-difluoromethoxy-4-chloro-3-(2-fluoro-4-chloro-5-nitrophenyl)pyrazole
https://huagongshe.com/reaction/634562
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | 1-Methyl-5-difluoromethoxy-4-chloro-3-(2-fluoro-4-chlorophenyl)pyrazole | HCID 11438328 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1-Methyl-5-difluoromethoxy-4-chloro-3-(2-fluoro-4-chloro-5-nitrophenyl)pyrazole | HCID 15672337 | 97.3% |
Reaction Steps
A mixture of 18.0 grams (0.058 mole) of 1-methyl-5-difluoromethoxy-4-chloro-3-(2-fluoro-4-chlorophenyl)pyrazole and 120 mL of concentrated sulfuric acid was stirred, and when the pyrazole was dissolved, the solution was cooled to 0° C. To this was added dropwise 5.5 mL (0.074 mole) of 70% nitric acid at a rate to maintain the reaction mixture temperature below 3° C. Upon completion of addition the reaction mixture was allowed to warm to about 10° C. where it stirred for two hours. After this time the reaction mixture was poured into ice-water and then extracted with several portions of diethyl ether. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 20.1 grams of 1-methyl-5-difluoromethoxy-4-chloro-3-(2-fluoro-4-chloro-5-nitrophenyl)pyrazole. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USH0001942H1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-87d97ec8f59f4ae7a27e0969e6e8f9b5 |
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| Source note | uspto-grants-2001_02 |
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