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HRID 482162作成日:2026年10月25日

Ethylene → 2-Vinyl-6-methoxynaphthalene

https://huagongshe.com/reaction/482162

反応式

関与物質

役割名称HCID仕込み量
反応物EthyleneHCID 6325—
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物2-Bromo-6-methoxynaphthaleneHCID 78786—
反応物Triethylammonium bromideHCID 2734074—
触媒Palladium ChlorideHCID 24290—
溶媒Ethyl ketoneHCID 7288—
生成物2-Vinyl-6-methoxynaphthaleneHCID 603535—

反応条件

温度95 °C

反応手順

To a 5-gallon stainless steel electrically heated reactor is added 1,485 grams (6.26 mol) of 2-bromo-6-methoxynaphthalene (BMN) (produced as in Example 7 hereof, added as a dry powder through a 2" opening in the reactor head), 672 grams (6.64 mol) of triethylamine, 0.56 grams of PdCl2 (3.2 mmol) and 6.2 grams of NMDP (19 mmol). The reactor is purged three times with nitrogen (50 psig) and then three times with ethylene (50 psig). The reactor is charged with ethylene (about 300 psig) and then warmed at 95° C. Ethylene pressure in the reactor is raised to about 550 psig after reaching reaction temperature. When the reaction is completed, the reaction mixture is cooled to below 50° C. and the ethylene is vented. Diethyl ketone (3,835 g) is added to the reaction mixture. Aqueous sodium hydroxide (24.8 wt %) is then added to the reaction mixture to neutralize the triethylamine hydrobromide salt formed during the reaction. The aqueous phase is removed, as well as possible at this point, from the reactor. The reaction mixture is filtered using a medium porosity 3-liter sintered glass funnel and any further aqueous phase that separates is removed. The volatile organics (acetonitrile, diethyl ketone, triethylamine) are removed at reduced pressure (1 mm Hg, 45° C.) to give 6-methoxy-2-vinylnaphthalene as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05792886
出典データセットuspto-grants-1998_08
ORD IDord-ed75f97fb4d04c68b12c8d5500858c77
出典メモuspto-grants-1998_08