HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381351Generated: November 4, 2026
Triethylamine → 2-(6-Oxo-1,6-dihydro-pyridazin-4-yloxy)-benzonitrile
https://huagongshe.com/reaction/2381351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 2-(6-Oxo-1,6-dihydro-pyridazin-4-yloxy)-benzamide | HCID 57919196 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(6-Oxo-1,6-dihydro-pyridazin-4-yloxy)-benzonitrile | HCID 57919184 | 87% |
Reaction Steps
A solution of 2-(6-oxo-1,6-dihydro-pyridazin-4-yloxy)-benzamide (31.1 g, 0.14 mol) in methylene chloride and triethylamine (65.5 g, 0.65 mol) was treated dropwise with trifluoroacetic anhydride (62.2 g, 0.30 mol). The resulting solution was stirred at 25° C. for 5 min. After this time, the reaction was washed with a 2N aqueous hydrochloric acid solution and a saturated aqueous sodium bicarbonate solution, dried over sodium sulfate, filtered, rinsed and concentrated in vacuo to afford 2-(6-oxo-1,6-dihydro-pyridazin-4-yloxy)-benzonitrile (25.1 g, 87%) as a white solid; ESI-MS 214 [M+H+]; HPLC: >95% (purity). 1H-NMR (300 MHz, CDCl3) δ 11.75 (s, 1H), 7.91 (s, 1H), 7.71-7.81 (m, 2H), 7.44-7.49 (m, 1H), 7.28-7.30 (m, 1H), 5.98 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258134B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-11c20d7f01a444688af276aee092bbe4 |
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| Source note | uspto-grants-2012_09 |
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