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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 632509생성일: 2026년 10월 26일

Butylamine → (1E,6E)-1,7-bis[4-(2-morpholinoethoxy)phenyl]hepta-1,6-diene-3,5-dione

https://huagongshe.com/reaction/632509

반응식

참여 물질

역할이름HCID투입량
반응물ButylamineHCID 8007—
반응물Potassium CarbonateHCID 11430—
반응물AcetylacetoneHCID 31261—
반응물4-(2-Morpholinoethoxy)benzaldehydeHCID 3719902—
반응물Boron monoxideHCID 6327189—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매Tributyl borateHCID 12712—
생성물(1E,6E)-1,7-bis[4-(2-morpholinoethoxy)phenyl]hepta-1,6-diene-3,5-dioneHCID 11788904324%

반응 조건

온도70 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321752B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-48d512c5912943118d34aa4458f6fa9f
출처 메모uspto-grants-2016_04