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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1694463Erstellt: 26. Oktober 2026

Bromobenzene → 5-Cyclohex-1-enyl-3-phenylamino-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1694463

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromobenzeneHCID 7961—
EduktCesium carbonateHCID 10796—
EduktBinap, (A+-)-HCID 634876—
Edukt5-Cyclohex-1-enyl-3-aminothiophene-2-carboxylic acid methyl esterHCID 57795401—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelDichloromethaneHCID 6344—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt5-Cyclohex-1-enyl-3-phenylamino-thiophene-2-carboxylic acid methyl esterHCID 5779536076%

Reaktionsschritte

To a solution of 5-cyclohex-1-enyl-3-amino-thiophene-2-carboxylic acid methyl ester (111 mg, 0.47 mmol) and bromobenzene (54 μL, 0.51 mmol) in dry dioxane (3 mL) were added cesium carbonate (459 mg, 1.41 mmol) and Pd2 dba3 (43 mg, 0.047 mmol), and the mixture was deoxygenated by bubbling nitrogen through solution for 10 min. Then BINAP (47 mg, 0.075 mmol) was added to the mixture, and it was refluxed under nitrogen overnight. The mixture was diluted with CH2Cl2 and filtered through celite washing with CH2Cl2. Filtrate was concentrated under reduced pressure and purified by column chromatography on silica gel eluting with 2-30% EtOAc in hexanes to give 111 mg (76%) of 5-cyclohex-1-enyl-3-phenylamino-thiophene-2-carboxylic acid methyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08158675B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-f80d7ba0be2c4cdabf5a81cdc401b9c6
Quellennotizuspto-grants-2012_04