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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1039469생성일: 2026년 10월 26일

4-(2-Propyn-1-yl)morpholine → methyl (E)-[2-methyl-4-[3-(2-methyl benzo[b]furan-5-yl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]-allyloxy]phenoxy]acetate

https://huagongshe.com/reaction/1039469

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참여 물질

역할이름HCID투입량
반응물4-(2-Propyn-1-yl)morpholineHCID 412941—
반응물methyl (Z)-[4-[3-(4-iodophenyl)-3-(2-methylbenzo[b]furan-5-yl)allyloxy]-2-methylphenoxy]acetateHCID 86629296—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매BenzeneHCID 241—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물methyl (E)-[2-methyl-4-[3-(2-methyl benzo[b]furan-5-yl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]-allyloxy]phenoxy]acetateHCID 86629295—

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온도0 °C

반응 단계

N-Propargylmorpholine (270 mg, 2.16 mmol) was added under nitrogen atmosphere to a degassed solution of methyl (Z)-[4-[3-(4-iodophenyl)-3-(2-methylbenzo[b]furan-5-yl)allyloxy]-2-methylphenoxy]acetate (400 mg, 0.68 mmol; prepared as described in example 25) in a mixture of tetrahydrofuran (6 mL) and triethylamine (6 mL). The solution was cooled to 0° C., tetrakis(triphenylphosphine)palladium (71 mg, 0.061 mmol) and copper(I) iodide (21 mg, 0.11 mmol) were added. The reaction mixture was stirred at ambient temperature for 96 h, diluted with benzene (100 mL), decanted and evaporated in vacuo. The residue was purified by column chromatography (silica gel Fluka 60, benzene/ethyl acetate 1:0-0:1) yielding methyl (E)-[2-methyl-4-[3(2-methylbenzo[b]furan-5-yl)-3-[4-[3-(morpholin-4-yl)propynyl]phenyl]-allyloxy]phenoxy]acetate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08551993B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-1bdfb73c464e4041b7d45065ff57e313
출처 메모uspto-grants-2013_10