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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl 2,4,6-trimethylbenzeneacetate | HCID 13524810 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 1-Dimethylamino-4-hydroxy-piperidine-4-carboxylic acid methyl ester | HCID 67225501 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 8-Dimethylamino-3-(2,4,6-trimethyl-phenyl)-1-oxa-8-aza-spiro[4.5]decane-2,4-dione | HCID 67226379 | 9.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08703165B2 |
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| 출처 데이터셋 | uspto-grants-2014_04 |
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| ORD ID | ord-c43e963e11744eefbc354d05535cbe47 |
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| 출처 메모 | uspto-grants-2014_04 |
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