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HRID 390692생성일: 2026년 10월 24일

Water → methyl (Z)-3-(3'-amino-2-butoxybiphenyl-4-yl)-2-methoxyacrylate

https://huagongshe.com/ko/reaction/390692

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물3-Aminophenylboronic acid hydrochlorideHCID 2763241—
반응물methyl (Z)-3-(3-butoxy-4-iodophenyl)-2-methoxyacrylateHCID 59574929—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
용매Ethyl AcetateHCID 8857—
생성물methyl (Z)-3-(3'-amino-2-butoxybiphenyl-4-yl)-2-methoxyacrylateHCID 8662612293.8%

반응 조건

온도100 °C

반응 단계

11.2 mL (22.4 mmol) of aqueous 2 N potassium carbonate solution and 0.52 g (0.45 mmol) of tetrakis(triphenylphosphine)palladium are added to a solution of 1.87 g (10.8 mmol) of 3-aminophenylboronic acid hydrochloride and 3.5 g (9 mmol) of methyl (Z)-3-(3-butoxy-4-iodophenyl)-2-methoxyacrylate (prepared according to Example 24c) in 70 mL of ethylene glycol dimethyl ether. The reaction mixture is heated at 100° C. for 4 hours. After addition of 30 mL of water and extraction with ethyl acetate, the organic phases are combined, washed with saturated sodium chloride solution and dried over sodium sulfate. The solvents are evaporated off and the residue is then purified by chromatography on a column of silica eluted with a 90/10 heptane/ethyl acetate mixture. 3 g (93%) of methyl (Z)-3-(3′-amino-2-butoxybiphenyl-4-yl)-2-methoxyacrylate are obtained in the form of a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383652B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-4f9266252fc34994bf2d41c1de451922
출처 메모uspto-grants-2013_02