참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isophorone | HCID 6544 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Sodium ethoxide | HCID 2723922 | — |
| 반응물 | 4-(Dibutylamino)-2-methoxybenzaldehyde | HCID 14643903 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-[2-(4-Dibutylamino-2-methoxyphenyl)vinyl]-5,5-dimethyl-2-cyclohexenone | HCID 68008965 | 45% |
반응 단계
In 15 ml of tetrahydrofuran, 1.5 g (10.85 mmol) of isophorone was dissolved, and 3.4 g of sodium ethoxide (20% solution in ethanol) (10.0 mmol) was added thereto. To this mixture, 2.6 g (9.87 mmol) of 4-dibutylamino-2-methoxybenzaldehyde in tetrahydrofuran was added dropwise with heating at 50° C., and the mixture was stirred for 4.5 hours. To the mixture, 100 ml of ethyl acetate was added. Washing with a saturated saline solution, drying over anhydrous sodium sulfate, and concentration were performed. The residue was purified by silica gel column chromatography to give 1.7 g of a reddish orange oily matter (yield: 45.0%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846955B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-19e301df09d24f28bc8d5a9e1c5a6ef8 |
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| 출처 메모 | uspto-grants-2014_09 |
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