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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1245434생성일: 2026년 10월 27일

Potassium Carbonate → Ethyl 2-{3'-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoate

https://huagongshe.com/reaction/1245434

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Benzoic acid, 2-fluoro-, ethyl esterHCID 67953—
반응물Tert-butyl(4'-hydroxybiphenyl-3-ylmethyl)methylcarbamateHCID 69643261—
용매WaterHCID 962—
용매DimethylacetamideHCID 31374—
생성물Ethyl 2-{3'-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoateHCID 21911050104.9%

반응 단계

2.15 g (12.8 mmol) of ethyl 2-fluorobenzoate and 1.9 g (14 mmol) of potassium carbonate are successively added to a solution of 4 g (12.8 mmol) of tert-butyl(4′-hydroxybiphenyl-3-ylmethyl)methylcarbamate in 45 ml of dimethylacetamide. The reaction medium is refluxed for 48 hours, cooled, diluted with water and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with an 80/20 heptane/ethyl acetate mixture. 3.1 g of ethyl 2-{3′-[(tert-butoxycarbonylmethylamino)methyl]biphenyl-4-yloxy}benzoate are obtained in the form of a colorless oil, in a yield of 53%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07125869B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-26c73ab41c454dd1858f0eff7961aaa0
출처 메모uspto-grants-2006_10