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HRID 1153843作成日:2026年10月27日

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

https://huagongshe.com/reaction/1153843

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物PhenylacetaldehydeHCID 998—
反応物MorpholineHCID 8083—
反応物ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylateHCID 76918—
溶媒TolueneHCID 1140—
生成物Ethyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylateHCID 1312628955.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04486588
出典データセットuspto-grants-1984_12
ORD IDord-34562dd3138241a699e716d8cd4ad8fd
出典メモuspto-grants-1984_12