HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409348Generated: October 27, 2026
Sodium Hydroxide → 1'H,2H-[3,3'-bipyrazole]-5-carboxylic acid
https://huagongshe.com/reaction/1409348
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 1'H,2H-[3,3'-bipyrazole]-5-carboxylate | HCID 70981238 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1'H,2H-[3,3'-bipyrazole]-5-carboxylic acid | HCID 17930753 | 157.9% |
Reaction Steps
Ethyl 1H,2′H-3,3′-bipyrazole-5-carboxylate (1.959 mmol, 0.404 g) was dissolved in ethanol (5 ml) and cooled in an ice bath. NaOH 1 M solution (1.959 mmol, 4 ml) was slowly added. The solution was heated to 60° C. for 1 h. Ethanol was removed under vacuum and the residue was diluted with tert-butyl methyl ether. The solution was again cooled with an ice bath and acidified with 2 N HCl solution. The solution was allowed to warm to ambient temperature and stirred overnight. Water and DCM was added and the phases were separated. Both phases were evaporated and combined. 0.551 g of the title compound was obtained. 1H-NMR (400 MHz, DMSO-d6): δ 6.70 (d, 1H), 7.04 (s, 1H), 7.77 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921378B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-ce013e2a37104dfca7d39c3e468768a0 |
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| Source note | uspto-grants-2014_12 |
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