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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571669Generated: October 30, 2026

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

https://huagongshe.com/reaction/571669

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 Step C) (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 numberUS09029365B2
Source datasetuspto-grants-2015_05
ORD IDord-4f2df8c87e9a45dc9f782707dceb1bb0
Source noteuspto-grants-2015_05