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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 467807Erstellt: 24. Oktober 2026

Hydrochloric Acid → Methyl 2-ethoxy-4-nitrobenzoate

https://huagongshe.com/de/reaction/467807

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl BromideHCID 6332—
EduktPotassium CarbonateHCID 11430—
EduktThionyl ChlorideHCID 24386—
Edukt4-Nitrosalicylic acidHCID 69266—
EduktSalicylic acid, 4-nitro-, methyl esterHCID 139539—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 2-ethoxy-4-nitrobenzoateHCID 996456626,2%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

4.05 g (21.7 mmol, 1 eq) 2-hydroxy-4-nitro-benzoic acid are dissolved in 40 mL MeOH and 1.8 mL (24.8 mmol, 1.14 eq) thionyl chloride are slowly added dropwise. The mixture is refluxed for 2 h at 50° C. and stirred for another 2 h. After cooling the volatile constituents are eliminated in vacuo and 4.36 g of the crude methyl 2-hydroxy-4-nitro-benzoate are obtained, which are reacted without further purification. 1 g (5.1 mmol, 1 eq) of the methyl ester are dissolved in 25 mL DMF, 2.1 g (15.3 mmol, 3 eq) potassium carbonate are added and then 1.4 mL (18.8 mmol, 3.7 eq) bromoethane are added dropwise. The reaction mixture is stirred for 16 h at RT, then poured into 100 mL water and the pH is adjusted with concentrated aqueous hydrochloric acid to pH 3. It is extracted twice with 100 mL EE, dried on MgSO4 and after the elimination of all the volatile constituents in vacuo 1.28 g of methyl 2-ethoxy-4-nitro-benzoate are obtained. 1.28 g (5.06 mmol, 1 eq) of the nitro compound are dissolved in 50 mL MeOH, a spatula tip of Raney nickel is added and the reaction mixture is stirred in the autoclave under a hydrogen pressure of 4 bar for 16 h. The catalyst is filtered off through Celite® and the filtrate is freed in vacuo of all the volatile constituents. 0.99 g of the aniline are obtained [MS-ESI+: 351 (M+H)+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08623887B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-7ad552fd00d54d15b842f50b5836d461
Quellennotizuspto-grants-2014_01