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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1260376생성일: 2026년 10월 26일

Triphenylphosphine → (E)-3-(3-hydroxy-4-methoxy-phenyl)-N-[3-(5-methyl-furan-2-ylmethoxy)-phenyl]-acrylamide

https://huagongshe.com/reaction/1260376

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물5-Methylfurfuryl alcoholHCID 520911—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물(E)-3-(3-acetoxy-4-methoxy-phenyl)-N-(3-hydroxy-phenyl)-acrylamideHCID 67340885—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물(E)-3-(3-hydroxy-4-methoxy-phenyl)-N-[3-(5-methyl-furan-2-ylmethoxy)-phenyl]-acrylamideHCID 453768651.7%

반응 단계

Diethylazodicarboxylate (1.13 mL 5.83 mmol) was added dropwise to a solution of (E)-3-(3-acetoxy-4-methoxy-phenyl)-N-(3-hydroxy-phenyl)-acrylamide (0.763 g, 2.33 mmol), (5-methyl-furan-2-yl)-methanol (0.392 g, 3.5 mmol) and triphenylphosphine (1.53 g, 5.83 mmol) in dry THF (20 mL) at 0° C. The resulting solution was allowed to reach RT and stirred for 16 hrs. The reaction mixture was then diluted with DCM and washed with water, aqueous hydrochloric acid, and brine. The organic layer was then dried over sodium sulphate and evaporated. The resulting raw material was taken up, without further purification, with a 3N methanolic solution of hydrochloric acid (5 mL-15 mmols) and stirred at RT for 16 hrs, concentrated under reduced pressure, taken up with solvent an re-evaporated (3 times with MeOH and once with acetone) to give a residue that was purified by silica gel column chromatography (eluant DCM/MeOH 98/2) to obtain 15 mg of the title (E)-3-(3-hydroxy-4-methoxy-phenyl)-N-[3-(5-methyl-furan-2-ylmethoxy)-phenyl]-acrylamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08470831B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-e24d35545ead4be29c57e45cb170b1d1
출처 메모uspto-grants-2013_06