참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Di-tert-butyl peroxide | HCID 8033 | — |
| 반응물 | Ethyl Acrylate | HCID 8821 | — |
| 반응물 | Cyclohexanol, 4,4-dimethyl- | HCID 136735 | — |
| 생성물 | 8,8-Dimethyl-1-oxa-spiro[4.5]decan-2-one | HCID 13409124 | 69.5% |
반응 단계
In a 500 ml three necked round bottom flask was charged 4,4-dimethyl-cyclohexanol (100 g, 0.78 mol) and heated up to 160° C., while adding over 4 hours tBuOOtBu (11.4 g, 0.08 mol) and ethylacrylate (39.2 g, 0.39 mol). 10 minutes after the end of the addition, the mixture was cooled to 50° C. and lights were distilled off. Then, 30% w/w aqueous NaOH (61 g) and MTBE (200 g) were added. Stirring was continued during the night at 40° C. and the aqueous phase was separated. The aqueous phase was re-extracted four times with MTBE (200 g). Afterwards, MTBE (200 g) was added to the aqueous phase, and the pH adjusted to 1 with 50% w/w aqueous H2SO4. The organic phase was washed with water and concentrated to yield 49.4 g of crude 8,8-dimethyl-1-oxa-spiro[4.5]decan-2-one (GC purity: 96.3%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06933265B2 |
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| 출처 데이터셋 | uspto-grants-2005_08 |
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| ORD ID | ord-233d41f352304ff683ba149e4246e80f |
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| 출처 메모 | uspto-grants-2005_08 |
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