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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1153843생성일: 2026년 10월 26일

Water → Ethyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylate

https://huagongshe.com/reaction/1153843

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물PhenylacetaldehydeHCID 998—
반응물MorpholineHCID 8083—
반응물ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylateHCID 76918—
용매TolueneHCID 1140—
생성물Ethyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylateHCID 1312628955.6%

반응 단계

A stirred solution of phenylacetaldehyde (77.0 g, 0.64 mole) and morpholine (56.0 g, 0.64 mole) in toluene (500 ml) was heated at reflux until the theoretical amount of water was collected in a Dean-Stark trap. The reaction mixture was cooled slightly, and ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate (125.0 g, 0.64 mole) was added. The solvent was distilled from the reaction mixture at atmospheric pressure to leave a residue. The residue was then heated at 200° for 2.5 hours. A Dean-Stark trap was used to collect the distilled morpholine. The remaining pot residue was cooled and slurried with a mixture of silica gel (700 g) and methylene chloride (1500 ml) for 45 minutes. The slurry was filtered and the filter cake rinsed with methylene chloride (500 ml). The combined filtrates were evaporated under reduced pressure to leave a thick brown residue. This residue was distilled under reduced pressure to give several fractions. All fractions which contained more than 73% product by gc analysis were combined to give a total of 90.5 g crude ethyl 2,4-dimethyl-[1,1'-biphenyl]-3-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04486588
출처 데이터셋uspto-grants-1984_12
ORD IDord-34562dd3138241a699e716d8cd4ad8fd
출처 메모uspto-grants-1984_12