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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 554767Erstellt: 25. Oktober 2026

Isobutyramide → HCID 29921637, Verbindung

https://huagongshe.com/reaction/554767

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsobutyramideHCID 68424—
Edukt5-Bromonicotinic acidHCID 88707—
Edukttert-Butyl 5-bromonicotinateHCID 18422124—
KatalysatorZinc cyanide (Zn(CN)2)HCID 11186—
KatalysatorZincHCID 23994—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
KatalysatorHCID 15826098HCID 15826098—
ProduktHCID 29921637HCID 29921637—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Instead of the starting material of Reference Example 56, that is, the compound S55, the 5-bromonicotinic acid was used for the similar procedure as in Reference Example 56. To the obtained tert-butyl 5-bromonicotinate (22.4 g), dimethylacetoamide (112 ml), tris(dibenzylideneacetone)dipalladium (1.59 g), zinc cyanide (6.1 g), diphenylphosphinoferrocene (1.92 g), and zinc powder (0.68 g) were added and the mixture was stirred under argon atmosphere at 120° C. for 1.5 hours. The reaction solution was filtered by sellite, which was then washed with ethyl acetate, and the filtrate was washed with saturated saline. The organic layer was dried over with anhydrous sodium sulfate, then concentrated. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=3/1) to obtain tert-butyl 5-cyanonicotinate (13.1 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08049006B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-f58ad093509a4dd39e2b73cc8e2e5615
Quellennotizuspto-grants-2011_11