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HRID 17539作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3,3-Dimethyl-1-butyneHCID 13512—
反応物Methyl 4-acetylamino-5-bromo-3-iodosalicylateHCID 86097515—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒1,4-DioxaneHCID 31275—
生成物Methyl 4-acetylamino-5-bromo-3-(3,3-dimethyl-1-butynyl)salicylateHCID 86630872—

反応条件

温度30 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737166B2
出典データセットuspto-grants-2010_06
ORD IDord-edb7512fe008400fbb309091a2445737
出典メモuspto-grants-2010_06