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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-(6-Oxo-1,6-dihydro-pyridazin-4-yloxy)-benzamideHCID 57919196—
SolventDichloromethaneHCID 6344—
Product2-(6-Oxo-1,6-dihydro-pyridazin-4-yloxy)-benzonitrileHCID 5791918487%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258134B2
Source datasetuspto-grants-2012_09
ORD IDord-11c20d7f01a444688af276aee092bbe4
Source noteuspto-grants-2012_09