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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 635603Erstellt: 25. Oktober 2026

Thiophene → Ethyl 4-[(5,5-dimethyl-8-(2-thienyl)-5,6-dihydronaphthalen-2-yl)azo]benzoate

https://huagongshe.com/reaction/635603

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiopheneHCID 8030—
EduktEthyl 4-[(5,6-dihydro-5,5-dimethyl-8-trifluoromethylsulfonyloxy-naphthalen-2-yl)azo]benzoateHCID 22323756—
EduktHCID 178418306HCID 178418306—
KatalysatorZincchlorideHCID 3007855—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelAmmonium ChlorideHCID 25517—
ProduktEthyl 4-[(5,5-dimethyl-8-(2-thienyl)-5,6-dihydronaphthalen-2-yl)azo]benzoateHCID 13006282—

Reaktionsschritte

To a cold solution (−78° C.) of thiophene (0.07 ml, 0.75 mmol) in 1.5 ml of THF was added t-BuLi (0.457 ml, 0.75 mmol, 1.7 M in pentane) and stirred for 2 h. To this solution, ZnCl2 (168 mg, 1.2 mmol) in 1.5 ml of THF was added. The resulting solution was warmed to room temperature, stirred for 1 h and was added (via cannula) to a solution of ethyl 4-[(5,6-dihydro-5,5-dimethyl-8-trifluoromethylsulfonyloxy-naphthalen-2-yl)azo]benzoate (Compound D11, 150 mg, 0.30 mmol) and tetrakis(triphenylphosphine)palladium(0) (10.6 mg) in 2.5 ml of THF. The resulting mixture was heated at 50° C. for 2.5 h. The reaction was diluted with sat. aqueous NH4Cl and extracted with ethyl acetate. The combined organic layer was dried over Na2SO4 and concentrated to an oil. The crude product was purified by flash chromatography (silica, ethyl acetate:hexane 5:95) to afford the title compound as a red foam.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06187933B1
Quelldatensatzuspto-grants-2001_02
ORD IDord-3a32589ab9e54138811a45a7813eb215
Quellennotizuspto-grants-2001_02