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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256841생성일: 2026년 10월 26일

Triethylamine → rac-3,4-Dihydro-2,5,7,8-tetramethyl-2-{[4-(3-pyridinyl)-phenyl]ethynyl}-2H-1-benzopyran-6-ol

https://huagongshe.com/reaction/256841

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TriphenylphosphineHCID 11776—
반응물3-(4-Iodophenyl)pyridineHCID 12644356—
반응물rac-3,4-dihydro-2-ethynyl-2,5,7,8-tetramethyl-2H-1-benzopyran-6olHCID 14478563—
용매AcetonitrileHCID 6342—
생성물rac-3,4-Dihydro-2,5,7,8-tetramethyl-2-{[4-(3-pyridinyl)-phenyl]ethynyl}-2H-1-benzopyran-6-olHCID 15171829—

반응 단계

A mixture of 1.15 g of rac-3,4-dihydro-2-ethynyl-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol, 1.14 g (4 mmol) of 3-(4-iodophenyl)pyridine, 0.2 g of triphenylphosphine, 50 mg of cuprous iodide, 1.5 ml of triethylamine and 20 ml of acetonitrile was degassed with argon for 10 minutes. Palladium acetate, 75 mg, was then added and stirring was continued for 3 hours. The reaction mixture was partitioned between methylene chloride and water. The organic layer was dried and evaporated. The residue was crystallized from ethyl acetate and recrystallized from methanol/ethyl acetate to give colorless crystals with m.p. 190°-192° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260294
출처 데이터셋uspto-grants-1993_11
ORD IDord-be389ac1631849338c0cc78715d1c37b
출처 메모uspto-grants-1993_11