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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80573Erstellt: 24. Oktober 2026

Pyridine → Tert-butyl 4-chloro-2-nitrobenzoate

https://huagongshe.com/de/reaction/80573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukttert-ButanolHCID 6386—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
Edukt4-Chloro-2-nitrobenzoic acidHCID 80475—
LösungsmittelTolueneHCID 1140—
ProduktTert-butyl 4-chloro-2-nitrobenzoateHCID 6389683288,7%

Reaktionsschritte

To 4-chloro-2-nitrobenzoic acid (262 g) in a pyridine (1.3 liter) solution, p-toluenesulfonyl chloride (272.6 g) was slowly added at room temperature, and the mixture was stirred at that temperature for 15 minutes. To the reaction solution, tert-butyl alcohol (249 ml) was added dropwise, then the mixture was stirred for 5 hours. To the reaction mixture toluene (1 liter) was added, and the mixture was stirred for 1.5 hours, then the precipitate were removed by filtration. The filtrate was concentrated, ethyl acetate (1.3 liter) was added to the residue, the mixture was successively washed with water, saturated aqueous potassium hydrogensulfate solution, aqueous saturated sodium hydrogencarbonate solution, and brine, then the organic layer was dried over anhydrous sodium sulfate, then concentrated. Methanol (470 ml) was added to the residue, and after the precipitation of the crystals was confirmed, water (142 ml) was added. The mixture was stirred under ice cooling for 1.5 hours, then the crystals were collected by filtration. The same recrystallization procedure as the above was performed again to obtain the title compound (297 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846660B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-550bcabf64c24c0a8f75ae8f00e583db
Quellennotizuspto-grants-2014_09