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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1054953Erstellt: 26. Oktober 2026

Dimethylformamide → 3-bromo-1-methyl-1H-1,2,4-triazole-5-carbaldehyde

https://huagongshe.com/reaction/1054953

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktHexaneHCID 8058—
Edukt3,5-Dibromo-1-methyl-1H-1,2,4-triazoleHCID 17186052—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-bromo-1-methyl-1H-1,2,4-triazole-5-carbaldehydeHCID 8466235655,3%

Reaktionsbedingungen

Temperatur-45 °C

Reaktionsschritte

To a solution of 3,5-dibromo-1-methyl-1H-1,2,4-triazole (500 mg, 2.08 mmol, Eq: 1.00) in tetrahydrofuran (5 ml) was added dropwise at −45° C. under argon atmosphere n-butyllithium 1.6 M in hexane (1.56 ml, 2.49 mmol, Eq: 1.2). The resulting mixture was stirred for 30 minutes at −45° C. and was then cooled to −70° C. Then dimethyl formamide (197 mg, 209 μl, 2.7 mmol, Eq: 1.3) was added dropwise. After 15 minutes the cooling bath was removed and the mixture was allowed to reach 25° C. The mixture was stirred for additional 2 hours at 25° C. The mixture was poured on water and extracted twice with ethyl acetate, the organic layers were combined, washed with water and brine, dried over magnesium sulfate, filtrated and evaporated, affording 5-bromo-2-methyl-2H-[1,2,4]triazole-3-carbaldehyde (218 mg/55.3%) as an orange semi solid. MS: m/e=189 (M+H+)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09394311B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-cd1494d8fc6a406eba7a47872be515f3
Quellennotizuspto-grants-2016_07