HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770894Generated: October 26, 2026
Hydrochloric Acid → 5-(But-2-ynyloxy)pyrazine-2-carboxylic acid
https://huagongshe.com/reaction/1770894
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Butyn-1-ol | HCID 12991 | — |
| Reactant | 5-Chloropyrazinoic acid | HCID 465472 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(But-2-ynyloxy)pyrazine-2-carboxylic acid | HCID 58448677 | 11.4% |
Reaction Steps
To a slurry of 5-chloro-pyrazine-2-carboxylic acid (0.79 g, 5.00 mmol) in DMF (35 mL) were added 2-butyn-1-ol (3.74 mL, 50.0 mmol) and potassium tert-butoxide (2.24 g, 20.0 mmol). The resulting mixture was heated at 65° C. overnight. The reaction mixture was neutralized with 2 M HCl and then concentrated in vacuo. A part (400 mg) of the crude material was partitioned between 0.5 M NaOH and a 1:1 mixture of heptane and EtOAc. The aqueous phase was made slightly acidic (pH-3-4) by addition of 1 M HCl. To the obtained suspension was added NaCl(s) and the mixture was extracted twice with EtOAc. The combined organic phases were dried (Na2SO4) and evaporated to give 0.11 g of the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.84 (t, 3H), 5.06 (q, 2H), 8.42 (d, 1H), 8.82 (d, 1H), 13.38 (br. s., 1H); MS (ES+) m/z 193 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09248129B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-989b22ccd2ae4c4f890627cf92dc825b |
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| Source note | uspto-grants-2016_02 |
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