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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255670Generated: November 1, 2026

Chloranil → HCID 20183850, compound

https://huagongshe.com/reaction/255670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloranilHCID 8371—
Reactant4-Amino-m-cresolHCID 17819—
ReactantHCID 57149955HCID 57149955—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 20183850HCID 2018385048.4%

Reaction Steps

In 5 ml of benzene was dissolved 0.3 g of methyl 5-cyclooctyl-3-oxo-4-pentenoate, and 0.3 g of N,N-dimethylformamidodimethylacetal was added thereto. They were reacted at 70° C. for one hour. Then, the reaction mixture was cooled to room temperature, and 0.27 g of 4-hydroxy-2-methylaniline was added thereto. The resulting mixture was subjected to reaction at room temperature for 2 hours. After completion of this reaction, the solvent was removed by distillation under reduced pressure, and the residue was purified by a column chromatography (Wako Silica Gel C-200; eluent: toluene/ethyl acetate (50:1 by volume) mixture). The fraction containing the objective substance was concentrated, and the oily substance thus obtained was dissolved in 5 ml of N,N-dimethylformamide and the resulting mixture was refluxed for 4 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and the residue was purified by a column chromatography (Wako Silica Gel C-200; eluent: chloroform/ethanol (50:1 by volume) mixture). The fraction containing the objective substance was concentrated and the oily substance thus obtained was dissolved in 5 ml of dioxane, and 0.2 g of 2,3,5,6-tetrachloro-p-benzoquinone was added thereto, and they were reacted at 80°-90° C. for 30 minutes. The reaction mixture was cooled to room temperature, and the precipitated crystals were collected by filtration. These crystals were dissolved in 20 ml of chloroform, and after removing the insolubles, the chloroform was removed by distillation under reduced pressure. To the residue was added 5 ml of a 1N aqueous sodium hydroxide solution and 5 ml of methanol, and they were reacted at room temperature for 30 minutes. After the methanol was removed by distillation under reduced pressure, the resulting solution was adjusted to a pH of 6.5 with 2N hydrochloric acid, and the precipitated crystals were collected by filtration, washed with water, and dried to obtain 0.14 g of 6-cyclooctyl-1-(4-hydroxy-2-methylphenyl)-4-oxo-1,4-dihydronicotinic acid having a melting point of 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698352
Source datasetuspto-grants-1987_10
ORD IDord-3f2bc03b5205443fa62df846f3eb35d9
Source noteuspto-grants-1987_10