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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 555429Erstellt: 26. Oktober 2026

2-Tert-Butylphenol → 2-(2-Tert-butylphenoxy)-3-nitrothiophene

https://huagongshe.com/reaction/555429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Tert-ButylphenolHCID 6923—
EduktPotassium CarbonateHCID 11430—
Edukt2-Chloro-3-nitrothiopheneHCID 220186—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt2-(2-Tert-butylphenoxy)-3-nitrothiopheneHCID 59857371—

Reaktionsbedingungen

Temperatur105 °C

Reaktionsschritte

To a solution of 2-chloro-3-nitrothiophene (1.13 g, 6.93 mmol) in NMP (10 mL) in a pressure vessel was added 2-tert-butylphenol (1.04 g, 6.93 mmol) and K2CO3 (1.0 g, 10.1 mmol). The reaction was flushed with nitrogen, sealed and then heated to 105° C. for 48 h. The reaction was cooled to rt, diluted with EtOAc (˜150 mL) and washed twice with saturated aqueous NaCl (2ט150 mL). The aqueous washes were then back extracted with EtOAc. The combined organics were dried over MgSO4, filtered and concentrated to yield the crude desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08053450B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-eb9dfcffa5234e0e81072bfdd967b62b
Quellennotizuspto-grants-2011_11