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HRID 1153842作成日:2026年10月27日

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

https://huagongshe.com/reaction/1153842

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylateHCID 76918—
反応物4-(2-Phenylethenyl)morpholineHCID 54492098—
溶媒TolueneHCID 1140—
生成物Ethyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylateHCID 1312628918.1%

反応手順

Under a dry nitrogen atmosphere a solution of commercial ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate (19.6 g, 0.1 mole) in toluene (20 ml) was added dropwise to a stirred solution of 4-(2-phenylethenyl)morpholine (14.3 g, 0.076 mole) in toluene (200 ml). Preparation of the morpholine derivative is described in U.S. Pat. No. 3,922,237. After the addition, the reaction mixture was heated at reflux for approximately 20 hours. The reaction mixture was then cooled and concentrated under reduced pressure, leaving a residue. The residue was heated at 170° under a dry nitrogen atmosphere for 3.5 hours, allowed to cool to room temperature, and then filtered. The filtrate was purified by column chromatography on silica gel, elution first with n-hexane: ethyl acetate, and finally ethyl acetate, to give ethyl 2,4-dimethyl-[1,1'-biphenyl]-3-carboxylate (3.5 g) as a yellow oil.

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-e52eceddde834449b16106a075d0035c
出典メモuspto-grants-1984_12