참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butylamine | HCID 8007 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Acetylacetone | HCID 31261 | — |
| 반응물 | 4-(2-Morpholinoethoxy)benzaldehyde | HCID 3719902 | — |
| 반응물 | Boron monoxide | HCID 6327189 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Tributyl borate | HCID 12712 | — |
| 생성물 | (1E,6E)-1,7-bis[4-(2-morpholinoethoxy)phenyl]hepta-1,6-diene-3,5-dione | HCID 117889043 | 24% |
반응 단계
To 2.0 g of pentane-2,4-dione were added 10.0 mL of AcOEt and 0.70 g of boron oxide, and the mixture was stirred at 70° C. for 1 hour. To the reaction mixture, 30 mL of a solution of 9.4 g of 4-(2-morpholinoethoxy)benzaldehyde in AcOEt and 10.7 mL of tributyl borate were successively added, and the mixture was stirred at the same temperature for 1 hour. To this, 0.4 mL of 1-butylamine was added, and the mixture was stirred at 70° C. for 2.5 hours and was allowed to cool back to room temperature. To the reaction mixture, 50 mL of a 10% K2CO3 aqueous solution and 30 mL of THF were added, and the mixture was stirred at room temperature for 10 minutes. The organic layer was separated, washed with saturated brine, dried over MgSO4, and concentrated. The residue was treated with 100 mL of diethyl ether to give 2.51 g of the title compound as a powder (24% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09321752B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-48d512c5912943118d34aa4458f6fa9f |
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| 출처 메모 | uspto-grants-2016_04 |
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