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HRID 29370作成日:2026年10月23日

1,2-Dimethoxyethane → 4-Furan-3-yl-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester

https://huagongshe.com/ja/reaction/29370

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物Potassium CarbonateHCID 11430—
反応物Furan-3-boronic acidHCID 2734358—
反応物3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl esterHCID 86599030—
溶媒WaterHCID 962—
生成物4-Furan-3-yl-3-methyl-benzofuran-2-carboxylic acid tert-butyl esterHCID 6871651368.4%

反応条件

温度85 °C

反応手順

3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl ester (285 mg, 0.75 mmol) was mixed with K2CO3 (207 mg, 2.2 eq), furan-3-boronic acid (101 mg, 1.2 eq), Pd(Ph3)4 (43 mg, 0.05 eq), 3 mL of 1,2-dimethoxyethane and 0.5 mL of water. The mixture was heated and stirred in a 85° C. oil bath for 2 h. The reaction mixture was poured into water and was extracted with ethyl acetate. The organic extract was washed with water and dried over sodium sulfate. Removal of the solvent in vacuo gave the crude product, which was purified by column chromatography to give 153 mg of 4-furan-3-yl-3-methyl-benzofuran-2-carboxylic acid tert-butyl ester, obtained as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420001B2
出典データセットuspto-grants-2008_09
ORD IDord-192bf958dc894ec9b93651037a8bedf4
出典メモuspto-grants-2008_09