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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51637생성일: 2026년 10월 24일

Tetrahydrofuran → [2-Fluoro-4-(8,8-dimethyl-5-oxo-5,6,7,8-tetrahydronaphthalene-2-ylethynyl)phenyl]acetic acid ethyl ester

https://huagongshe.com/ko/reaction/51637

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Ethyl AcetateHCID 8857—
반응물Ethyl 2-fluoro-4-iodophenylacetateHCID 18740710—
반응물6-ethynyl-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-oneHCID 22568823—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매HexaneHCID 8058—
생성물[2-Fluoro-4-(8,8-dimethyl-5-oxo-5,6,7,8-tetrahydronaphthalene-2-ylethynyl)phenyl]acetic acid ethyl esterHCID 69548870—

반응 단계

Following general procedure F and using 6-ethynyl-4,4-dimethyl-1,2,3,4-tetrahydro-naphthalene-1-one (Intermediate 13, 0.298 g, 1.43 mmol), 2-fluoro-4-iodo phenyl acetic acid ethyl ester (Reagent C, 0.44 g, 1.43 mmol), triethyl amine (Intermediate 13, 3 mL), anhydrous tetrahydrofuran (7 mL), copper(I)iodide (0.04 g, 0.2 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.15 g, 0.213 mmol) followed by flash column chromatography over silica gel (230-400 mesh) using 14-16% ethyl acetate in hexane as the eluent, the title compound was obtained as an oil (0.43 g, 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713647B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-326e61240f25487ead295b63635cdfe4
출처 메모uspto-grants-2004_03