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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2367896생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 2,4,6-trimethylbenzeneacetateHCID 13524810—
반응물Potassium tert-butoxideHCID 23665647—
반응물1-Dimethylamino-4-hydroxy-piperidine-4-carboxylic acid methyl esterHCID 67225501—
용매TetrahydrofuranHCID 8028—
생성물8-Dimethylamino-3-(2,4,6-trimethyl-phenyl)-1-oxa-8-aza-spiro[4.5]decane-2,4-dioneHCID 672263799.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08703165B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-c43e963e11744eefbc354d05535cbe47
출처 메모uspto-grants-2014_04