HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694613Generated: October 29, 2026
HCID 22172777, compound → Ethyl 1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylate
https://huagongshe.com/reaction/1694613
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22172777 | HCID 22172777 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylate | HCID 22172778 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158802B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-a4be0570440e46808ed3ffca54d78104 |
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| Source note | uspto-grants-2012_04 |
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