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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 906154Erstellt: 24. Oktober 2026

Cesium carbonate → (R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoate

https://huagongshe.com/de/reaction/906154

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt(R)-sec-butylamineHCID 2724537—
EduktMethyl 4-cyano-5-iodo-2-methylbenzoateHCID 67402433—
EduktBis(diphenylphosphino)xantheneHCID 86631950—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoateHCID 6740484973,4%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

To a solution of methyl 4-cyano-5-iodo-2-methylbenzoate (500 mg, 1.66 mmol) in 1,4-dioxane (25 mL) was added 9,9-dimethyl-4,5-(bis(diphenylphosphino)xanthene (96 mg, 0.166 mmol), tris(dibenzylideneacetone)-dipalladium (76 mg, 0.083 mmol), cesium carbonate (1.08 g, 3.32 mmol) and (R)-butan-2-amine (506 μL, 4.98 mmol). The reaction mixture was heated to 95° C. and stirred for 16 h, at which time it was cooled to room temperature. The heterogeneous mixture was filtered through a bed of celite, and the filter cake rinsed with ethyl acetate. The filtrate was concentrated, and the residue was purified by flash chromatography (100% hexanes to 5% ethyl acetate in hexanes) to afford (R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoate (300 mg, 73%) as a bright yellow oil. MS (EI) for C14H18N2O2: 247 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08012956B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-56f4bd5e5abc4c9cb6205e213034de88
Quellennotizuspto-grants-2011_09