関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Dimethylmalonyl Dichloride | HCID 4523180 | — |
| 反応物 | N-(2-ChlorobenZyl)hydroxylamine | HCID 12811040 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-((2-Chlorophenyl)methyl)-4,4-dimethyl-1,2-oxazolidine-3,5-dione | HCID 12811046 | 29.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04302238 |
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| 出典データセット | uspto-grants-1981_11 |
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| ORD ID | ord-23662a6ffb944885b11e5ec0f2fc422a |
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| 出典メモ | uspto-grants-1981_11 |
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