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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16760Erstellt: 23. Oktober 2026

Cesium carbonate → Tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylate

https://huagongshe.com/de/reaction/16760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt2-AcetylcyclohexanoneHCID 13400—
EduktMethyl 4-iodobenzoateHCID 69273—
EduktTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
KatalysatorCopper iodideHCID 83717—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylateHCID 5736268413,2%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Methyl 4-iodobenzoate (1.00 g, 3.82 mmol, 1.0 eq) was dissolved in DMF and tert-butyl 1,4-diazepane-1-carboxylate (765 mg, 3.82 mmol, 1.0 eq), caesium carbonate (2.49 g, 7.63 mmol, 2.0 eq), 2-acetylcyclohexanone (101 μl, 0.76 mmol, 0.20 eq [20 mol %]) and copper iodide (37 mg, 0.19 mmol, 0.05 eq [5 mol %]) were added. The reaction mixture was stirred at 90° C. under nitrogen for 7 h. The reaction mixture was evaporated, dissolved in DCM (50 ml), washed with water (20 ml), saturated ammonium chloride solution (20 ml), dried over MgSO4, filtered and evaporated. The crude product was purified by silica column chromatography, eluting with 0-1% MeOH in DCM. The product containing fractions were combined, evaporated and dried in vacuo to give tert-butyl 4-(4-methoxycarbonylphenyl)-1,4-diazepane-1-carboxylate (168 mg, 13%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-bf580b2f31564622a5397ead6f2f9ef0
Quellennotizuspto-grants-2010_06