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HRID 387490作成日:2026年10月25日

Ammonium Chloride → 2-Methoxy-1-phenylnaphthalene

https://huagongshe.com/reaction/387490

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Phenylboronic AcidHCID 66827—
反応物1-Bromo-2-methoxynaphthaleneHCID 72860—
触媒TriphenylphosphineHCID 11776—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-Methoxy-1-phenylnaphthaleneHCID 1132226666%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372996B2
出典データセットuspto-grants-2013_02
ORD IDord-36571d0ab94e4cce8539905db4773d03
出典メモuspto-grants-2013_02