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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414428Generated: October 30, 2026

Benzene → HCID 53890094, compound

https://huagongshe.com/reaction/414428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantTriethylamineHCID 8471—
Reactant5-nitrosoquinolin-6-olHCID 279598—
ReactantHCID 21280651HCID 21280651—
SolventWaterHCID 962—
ProductHCID 53890094HCID 538900942.8%

Reaction Steps

Into a dry 250 ml three-necked flask kept under dry nitrogen and fitted with a distillation column and internal thermometer was added 2-phenoxymethyl-3,4,4-trimethyl-1,3-oxazolidinium iodide (6.00 grams, 18.1 mmole) and 80 ml dry benzene. To the heterogeneous stirred solution was added in one portion triethylamine (3.64 grams, 36 mmole) followed by 5-nitroso-6-quinolinol (2.61 grams, 15 mmole). The solution was heated to reflux and maintained at reflux for 3 hours during which time water that formed during the course of the reaction was azeotropically removed. The solution was cooled with stirring overnight, decanted away from the tarry residue, and concentrated in vacuo. The product was isolated by flash chromatography to yield 0.16 grams of 2'-phenoxy-3,4,4-trimethylspiro[oxazolidine-2,3'-[3H]pyrido[3,2-f] [1,4]benzoxazine], which was characterized by appropriate spectral techniques. A toluene solution of the product changed to red when irradiated with ultraviolet light. The solution returned to its original hue after the UV light was removed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792224
Source datasetuspto-grants-1988_12
ORD IDord-a0223fa9d4fa415b81c229de18947dc9
Source noteuspto-grants-1988_12