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HRID 596319作成日:2026年10月26日

Dicyclohexylcarbodiimide → 4-(5-Chloro-2-methoxy-anilino-carbonyl-methyl)-4'-hydroxybiphenyl

https://huagongshe.com/reaction/596319

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物5-Chloro-2-methoxyanilineHCID 66763—
反応物(1,1'-Biphenyl)-4-acetic acid, 4'-hydroxy-HCID 603371—
溶媒TetrahydrofuranHCID 8028—
溶媒1,4-DioxaneHCID 31275—
生成物4-(5-Chloro-2-methoxy-anilino-carbonyl-methyl)-4'-hydroxybiphenylHCID 7063772870%

反応手順

A solution of 10 gm (44 millimols) of 4-hydroxy-4'-biphenyl-acetic acid (see W. H. Linnell and H. J. Smith, J. Chem. Soc. 1959,557) in a mixture of 33 ml of tetrahydrofuran and 162 ml of absolute dioxane were added at 0° C to a solution of 4.63 gm (29.4 millimols) of 2-methoxy-5-chloroaniline (m.p. 83°-85° C) in 40 ml of absolute dioxane, and the mixed solution was subsequently admixed with a solution of 9.1 gm (44 millimols) of N,N'-dicyclohexyl-carbodiimide in 20 ml of dioxane. After 20 hours of reaction time at 0° C, the dicyclohexylurea was filtered off and the solvent was distilled off. The residue was dissolved in 700 ml of chloroform, the solution was washed several times with 2N hydrochloric acid and water, dried over sodium sulfate, and the organic phase was evaporated in vacuo. The light brown, viscous crude product was purified on a silicagel column with toluene/acetic acid (4:1 ) as the eluant. Yield: 70% of theory; m.p. 165°-168° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04010279
出典データセットuspto-grants-1977_03
ORD IDord-627ff893c6de4ec6ad39336ad49d6e68
出典メモuspto-grants-1977_03