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HRID 2367896作成日:2026年10月25日

Methyl 2,4,6-trimethylbenzeneacetate → 8-Dimethylamino-3-(2,4,6-trimethyl-phenyl)-1-oxa-8-aza-spiro[4.5]decane-2,4-dione

https://huagongshe.com/reaction/2367896

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 2,4,6-trimethylbenzeneacetateHCID 13524810—
反応物Potassium tert-butoxideHCID 23665647—
反応物1-Dimethylamino-4-hydroxy-piperidine-4-carboxylic acid methyl esterHCID 67225501—
溶媒TetrahydrofuranHCID 8028—
生成物8-Dimethylamino-3-(2,4,6-trimethyl-phenyl)-1-oxa-8-aza-spiro[4.5]decane-2,4-dioneHCID 672263799.3%

反応手順

To a degassed solution of 0.5 g (2,4,6-trimethyl-phenyl)-acetic acid methyl ester and 0.63 g 1-dimethylamino-4-hydroxy-piperidine-4-carboxylic acid methyl ester in 20 ml tetrahydrofuran is added under argon at room temperature 5.72 ml of a 1M potassium tert-butoxide solution in tetrahydrofuran dropwise. The reaction mixture is stirred at room temperature for one hour, and at reflux overnight. The solvent is evaporated, the residue poured into ice/water and the pH adjusted to 5-6 by addition of aqueous 2N hydrochloric acid. The water phase is extracted with diethyl ether, the combined organic layer dried over sodium sulfate, and the solvent evaporated. The crude residue (910 mg) is purified several times by chromatography (normal and reversed phase systems) to yield pure 8-Dimethylamino-3-(2,4,6-trimethyl-phenyl)-1-oxa-8-aza-spiro[4.5]decane-2,4-dione (80 mg) as a solid with mp>200° C. 1H-NMR (DMSO-d6): 6.86 ppm (s, 2H), 2.93 ppm (m, 2H), 2.63 ppm (m, 2H), 2.38 ppm (s, 6H), 2.23 ppm (s, 3H), 2.12 ppm (m, 2H), 2.03 ppm (s, 6H), 1.60 ppm (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08703165B2
出典データセットuspto-grants-2014_04
ORD IDord-c43e963e11744eefbc354d05535cbe47
出典メモuspto-grants-2014_04