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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 387490Erstellt: 23. Oktober 2026

Ammonium Chloride → 2-Methoxy-1-phenylnaphthalene

https://huagongshe.com/de/reaction/387490

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktPhenylboronic AcidHCID 66827—
Edukt1-Bromo-2-methoxynaphthaleneHCID 72860—
KatalysatorTriphenylphosphineHCID 11776—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt2-Methoxy-1-phenylnaphthaleneHCID 1132226666%

Reaktionsschritte

To a flask charged with 1-bromo-2-methoxynaphthalene (20.0 g, 84.4 mmol), phenylboronic acid (11.3 g, 92.8 mmol), palladium acetate (0.10 g, 0.46 mmol), triphenylphosphine (0.85 g, 2.78 mmol) and potassium phosphate (40.9 g, 177.9 mmol), added was mixture of water (60 mL) and dimethoxyethane (120 mL), and the resultant mixture was heated under reflux for 6 hours. After cooling the mixture to ambient temperature, aqueous ammonium chloride solution (150 mL) and diethyl ether (200 mL) were injected thereto. The organic layer was isolated, and the residue was extracted with diethyl ether. The combined organic layer was dried over magnesium sulfate and evaporated to remove the volatile substances. Purification via silica gel column chromatography (n-hexane) gave 2-methoxy-1-phenylnaphthalene (13.0 g, yield: 66%) as colorless liquid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08372996B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-36571d0ab94e4cce8539905db4773d03
Quellennotizuspto-grants-2013_02