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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1673349Erstellt: 24. Oktober 2026

t-Butyl bromide → Tert-butyl 2-nitro-4-phenoxybenzoate

https://huagongshe.com/de/reaction/1673349

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktt-Butyl bromideHCID 10485—
EduktPotassium CarbonateHCID 11430—
EduktDimethylacetamideHCID 31374—
Edukt2-Nitro-4-phenoxybenzoic acidHCID 17989326—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 2-nitro-4-phenoxybenzoateHCID 67342192—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

9.9 g of potassium carbonate, 0.82 g of benzyltriethyl-ammonium chloride and 21 mL of 2-bromo-2-methylpropane were added to 14 mL of N,N-dimethylacetamide solution containing 0.93 g of 2-nitro-4-phenoxybenzoic acid at room temperature and stirred at 55° C. for 18 hours. After the reaction mixture was cooled to room temperature, water and ethyl acetate were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium hydrogen carbonate aqueous solution, 10% citric acid aqueous solution and a saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure to obtain 0.86 g of tert-butyl 2-nitro-4-phenoxybenzoate as white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07999132B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-9b0ee9658cf344ea805af8881975cceb
Quellennotizuspto-grants-2011_08