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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 596319Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/596319

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt5-Chloro-2-methoxyanilineHCID 66763—
Edukt(1,1'-Biphenyl)-4-acetic acid, 4'-hydroxy-HCID 603371—
LösungsmittelTetrahydrofuranHCID 8028—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-(5-Chloro-2-methoxy-anilino-carbonyl-methyl)-4'-hydroxybiphenylHCID 7063772870%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04010279
Quelldatensatzuspto-grants-1977_03
ORD IDord-627ff893c6de4ec6ad39336ad49d6e68
Quellennotizuspto-grants-1977_03