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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2185885Erstellt: 25. Oktober 2026

Oxalyl chloride → Methyl 3-hydroxynaphthalene-1-carboxylate

https://huagongshe.com/reaction/2185885

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt3-Hydroxy-1-naphthoic acidHCID 190232—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 3-hydroxynaphthalene-1-carboxylateHCID 2342309035%

Reaktionsschritte

To a stirred solution of 3-hydroxy-1-naphthalenecarboxylic acid (6.67 g, 35.4 mmol) and oxalyl chloride (3.86 mL, 44.2 mmol) in DCM (150 mL) was added 3 drops of DMF. The mixture was stirred at room temperature for 3 h., the solvent was removed under reduced pressure and methanol (150 mL) was added. After stirring at reflux for 15 min the solvent was removed under reduced pressure, the residue was purified by column chromatography (10%, 20% and 30% EtOAc/hexane) to give the title compound as a yellow solid (2.5 g, 35%). 1H NMR (DMSO-d6) δ 10.10 (s, 1H), 8.61 (d, 1H), 7.77 (d, 1H), 7.72 (d, 1H), 7.47 (m, 2H), 7.38 (d, 1H), 3.93 (s, 3H); MS m/z 201.1 (M−H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06403601B1
Quelldatensatzuspto-grants-2002_06
ORD IDord-6f31a575f07b468da6155b9f28e6b5a0
Quellennotizuspto-grants-2002_06