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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17539생성일: 2026년 10월 24일

Triethylamine → Methyl 4-acetylamino-5-bromo-3-(3,3-dimethyl-1-butynyl)salicylate

https://huagongshe.com/ko/reaction/17539

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,3-Dimethyl-1-butyneHCID 13512—
반응물Methyl 4-acetylamino-5-bromo-3-iodosalicylateHCID 86097515—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물Methyl 4-acetylamino-5-bromo-3-(3,3-dimethyl-1-butynyl)salicylateHCID 86630872—

반응 조건

온도30 °C

반응 단계

Under nitrogen atmosphere, methyl 4-acetylamino-5-bromo-3-iodosalicylate (I-250) (414 mg, 1.0 mmol), bis(triphenylphosphine)palladium(II) chloride (49 mg, 0.07 mmol), copper(I) iodide (19 mg, 0.1 mmol) and 3,3-dimethyl-1-butyne (0.13 ml, 1.1 mmol) were added to a mixed liquid of triethylamine (4 ml) and dioxane (6 ml), followed by stirring at 30° C. for 2 hours. The reaction liquid was concentrated under reduced pressure, then saturated ammonium chloride water was added to the residue, followed by extraction twice with chloroform, the organic layer was washed with saturated brine, then dried over anhydrous magnesium sulfate. After filtration and concentration under reduced pressure, the resulting residue was subjected to column, chromatography, and the eluate with n-hexane/ethyl acetate (2:1) gave the entitled compound (243 mg, 66.5) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-edb7512fe008400fbb309091a2445737
출처 메모uspto-grants-2010_06