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HRID 1155462作成日:2026年10月25日

Triethylamine → 2-((2-Chlorophenyl)methyl)-4,4-dimethyl-1,2-oxazolidine-3,5-dione

https://huagongshe.com/reaction/1155462

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Dimethylmalonyl DichlorideHCID 4523180—
反応物N-(2-ChlorobenZyl)hydroxylamineHCID 12811040—
溶媒TolueneHCID 1140—
生成物2-((2-Chlorophenyl)methyl)-4,4-dimethyl-1,2-oxazolidine-3,5-dioneHCID 1281104629.8%

反応手順

To a stirred solution of 8.3 grams (0.053 mole) of N-(2-chlorophenylmethyl)hydroxylamine and 12.1 grams (0.12 mole) of triethylamine in 200 ml of dry toluene was added dropwise a solution of 9.0 grams (0.053 mole) of dimethylmalonyl chloride in 50 ml of dry toluene. The addition required approximately 30 minutes and caused a white precipitate to form. The reaction mixture was stirred at room temperature for about 16 hours. The white precipitate was collected by filtration and washed with toluene. The combined wash and filtrate was washed with two portions of water and one portion of an aqueous solution saturated with sodium chloride and then dried with sodium sulfate. The solution was filtered from the sodium sulfate, and the filtrate was concentrated under reduced pressure to a viscous liquid. The liquid was subjected to column chromatography on silica gel. Elution was accomplished with 15% ethyl acetate in hexane. The fractions showing product by thin layer chromatography were combined to give an oil, which was distilled under reduced pressure to give 4.0 grams of 2-[(2-chlorophenyl)methyl]-4,4-dimethylisoxazolidine-3,5-dione; bp 115° C./0.03 mm. The nmr and the ir spectra were consistent with the assigned structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04302238
出典データセットuspto-grants-1981_11
ORD IDord-23662a6ffb944885b11e5ec0f2fc422a
出典メモuspto-grants-1981_11