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HRID 29370생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Potassium CarbonateHCID 11430—
반응물Furan-3-boronic acidHCID 2734358—
반응물3-Methyl-4-trifluoromethanesulfonyloxy-benzofuran-2-carboxylic acid tert-butyl esterHCID 86599030—
용매WaterHCID 962—
생성물4-Furan-3-yl-3-methyl-benzofuran-2-carboxylic acid tert-butyl esterHCID 6871651368.4%

반응 조건

온도85 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-192bf958dc894ec9b93651037a8bedf4
출처 메모uspto-grants-2008_09