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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620768Generated: October 31, 2026

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

https://huagongshe.com/reaction/620768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantDiethyl EtherHCID 3283—
ReactantBoron trifluorideHCID 6356—
ReactantHCID 13650289HCID 13650289—
SolventTolueneHCID 1140—
Product4H-3,1-Benzoxazin-4-one, 2,2'-(2-phenylethenylidene)bis-HCID 3063813—

Reaction Steps

Benzaldehyde 259 mg, 2.45 mmol), Compound (2,2'-methylenebis(3,1-benzoxazine-4-one) (500 mg, 1.63 mmol), and BF3.(C2H5)2O (0.045 ml, 0.163 mmol) where heated under reflux in dry toluene (20 ml) for 20 hours. After the reaction, the solvent was removed under reduced pressure from the reaction mixture, the residue was treated with water, extracted with benzene, and the organic layer was separated, washed with water and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in the developing solvent and adsorbed on silica gel, and was purified by column chromatography to give the desired compound 52. The obtained product was crystallized from isopropylether to give the desired compound 52 in white solid in a good yield. 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-7e7bca120a924bd79315c4956321c23c
Source noteuspto-grants-1989_04