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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620767Generated: October 30, 2026

Triethylamine → 4H-3,1-Benzoxazin-4-one, 2,2'-(2-phenylethenylidene)bis-

https://huagongshe.com/reaction/620767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
ReactantBenzoic acid, 2,2'-((1,3-dioxo-2-(phenylmethylene)-1,3-propanediyl)diimino)bis-HCID 3062455—
SolventDichloromethaneHCID 6344—
Product4H-3,1-Benzoxazin-4-one, 2,2'-(2-phenylethenylidene)bis-HCID 3063813—

Reaction Conditions

Temperature40 °C

Reaction Steps

Under nitrogen gas current, 2-chloro-N-methylpyridinium iodide (691 mg, 2.78 mmol) was suspensed in dry methylene chloride (5 ml) and a solution of Compound 11 (500 mg, 1.16 mmol) and dry triethylamine (0.76 ml, 5.57 mmol) in dry methylene chloride (5 ml) were added. The mixture was stirred at 40° C. for 3.5 hours. After the reaction, methylene chloride was added, and the mixture was washed with 1N.HCl, water, 4% NaHCO3 aqueous solution and water and dried over magnesium sulfate. The solvent was evaporated. The residue was crystallized rrcm isopropylether to give the desired compound 52 in crystal (410 mg, yield, 90%). m.p., IR, and NMR spectra of the product fully agreed with those of the one obtained in Example 19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822791
Source datasetuspto-grants-1989_04
ORD IDord-e8b9c8be6d674d00b5a19b089560c216
Source noteuspto-grants-1989_04