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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823336Generated: November 2, 2026

HCID 22172777, compound → Ethyl 1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1823336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22172777HCID 22172777—
CatalystSulfuric AcidHCID 1118—
SolventAcetic AcidHCID 176—
ProductEthyl 1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylateHCID 2217277877%

Reaction Conditions

Temperature65 °C

Reaction Steps

Sulfuric acid (concentrated, 2 drops) was added to ethyl 1-(3-chloro-2-pyridinyl)-4,5-dihydro-5-hydroxy-3-(trifluoromethyl)-1H-pyrazole-5-carboxylate (i.e. the product of Example 3) (1 g, 2.96 mmol) in acetic acid (10 mL) and the mixture was warmed to 65° C. for about 1 hour. The mixture was allowed to cool to 25° C. and most of the acetic acid was removed under reduced pressure. The mixture was partitioned between saturated aqueous sodium carbonate solution (100 mL) and ethyl acetate (100 mL). The aqueous layer was further extracted with ethyl acetate (100 mL). The combined organic extracts were dried and evaporated to give the product as an oil (0.66 g, 77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07038057B2
Source datasetuspto-grants-2006_05
ORD IDord-fef5f411d73846ec99c2a041d288c4df
Source noteuspto-grants-2006_05