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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1771459Erstellt: 27. Oktober 2026

Methyl 4-(1-bromo-6-methoxynaphthalen-2-yl)benzoate → Methyl 4-(6-methoxy-1-methylnaphthalen-2-yl)benzoate

https://huagongshe.com/reaction/1771459

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-(1-bromo-6-methoxynaphthalen-2-yl)benzoateHCID 67974719—
EduktHCID 178477798HCID 178477798—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 4-(6-methoxy-1-methylnaphthalen-2-yl)benzoateHCID 6797496885%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of methyl 4-(1-bromo-6-methoxynaphthalen-2-yl)benzoate (300 mg, 0.811 mmol) (see Example 12 step 1), MeZnCl (1.2 mL, 2.40 mmol, 2M in THF) and Pd(PPh3)4 (93.8 mg, 0.0811 mmol) in anhydrous THF (10 mL) was stirred at 60° C. under N2 atmosphere for 16 hours. After cooling to room temperature, the mixture was quenched with saturated aqueous NH4Cl (20 mL), extracted with EtOAc (20 mL×3). The combined organic layers were washed with H2O (20 mL) and brine (20 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column (PE/EtOAc=300/1 to 200/1) to give the product (210 mg, yield 85%) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09249132B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-b88c74d2a79246f7acf9fe564c887fdb
Quellennotizuspto-grants-2016_02