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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1914691Erstellt: 27. Oktober 2026

2-(4-Methoxy-2-nitrophenyl)acetic acid → 2-(4-Methoxy-2-nitrophenyl)ethan-1-ol

https://huagongshe.com/reaction/1914691

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(4-Methoxy-2-nitrophenyl)acetic acidHCID 11413180—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(4-Methoxy-2-nitrophenyl)ethan-1-olHCID 1983553594%

Reaktionsschritte

To a solution of (4-methoxy-2-nitrophenyl)acetic acid (400 mg; 1.9 mmol; 1 eq) in THF (10 mL) at 0° C. is added slowly under nitrogen borane-tetrahydrofuran complex (4.74 mL; 1 M; 4.7 mmol; 2.5 eq) and the reaction is stirred overnight at room temperature. No conversion is observed. The reaction mixture is heated at 70° C. for 2 h. The reaction is quenched by addition of water and the expected product is extracted with EtOAc. The organic phase is dried over MgSO4 and the solvent removed under reduced pressure. The residue obtained is purified by the flash chromatography using cyclohexane/EtOAc (7/3) as eluent to afford 350 mg (94%) of the title compound as a yellow oil. 1H NMR (CDCl3) δ 7.20 (d, J=3.0 Hz, 1H), 7.06 (d, J=8.0 Hz, 1H), 6.85 (dd, J=8.0, 3.0 Hz, 1H), 3.66 (t, J=9.0 Hz, 2H), 3.61 (s, 3H), 2.86 (t, J=9.0 Hz, 2H), 1.88 (br s, 1H). HPLC (max plot) 100%; Rt 2.48 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08614215B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-30011162150b4012ad75e34acfb79ea2
Quellennotizuspto-grants-2013_12