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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | Benzoic acid, 2,2'-((1,3-dioxo-2-(phenylmethylene)-1,3-propanediyl)diimino)bis- | HCID 3062455 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4H-3,1-Benzoxazin-4-one, 2,2'-(2-phenylethenylidene)bis- | HCID 3063813 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822791 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-e8b9c8be6d674d00b5a19b089560c216 |
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| Source note | uspto-grants-1989_04 |
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