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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1795113Erstellt: 24. Oktober 2026

1-Chloromethylnaphthalene → 2-(Naphthalen-1-ylmethoxy)benzaldehyde

https://huagongshe.com/de/reaction/1795113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-ChloromethylnaphthaleneHCID 6845—
EduktSalicylaldehydeHCID 6998—
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(Naphthalen-1-ylmethoxy)benzaldehydeHCID 88549643,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 2-hydroxybenzaldehyde (2.30 g, 18.8 mmol) in DMF (20 mL) is added 1-(chloromethyl)-naphthalene (3.36 mL, 22.6 mmol) and K2CO3 (3.11 g, 22.6 mmol), and the reaction mixture is heated to 100° C. for 12 h. Once complete, the reaction mixture is cooled to room temperature and diluted with water (100 mL) prior to being poured into a separatory funnel containing ethyl acetate (250 mL). The organic layer is separated, washed with brine (2×) and dried over sodium sulfate prior to concentration. The crude product is purified by column chromatography (5% ethyl acetate in hexanes) to afford 2-(1-naphthylmethoxy)benzaldehyde (2.13 g, 43%) as a light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07026339B2
Quelldatensatzuspto-grants-2006_04
ORD IDord-3f39b2fc764a4dc582d690e962a26da4
Quellennotizuspto-grants-2006_04