돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 482162생성일: 2026년 10월 24일

Ethylene → 2-Vinyl-6-methoxynaphthalene

https://huagongshe.com/ko/reaction/482162

반응식

참여 물질

역할이름HCID투입량
반응물EthyleneHCID 6325—
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물2-Bromo-6-methoxynaphthaleneHCID 78786—
반응물Triethylammonium bromideHCID 2734074—
촉매Palladium ChlorideHCID 24290—
용매Ethyl ketoneHCID 7288—
생성물2-Vinyl-6-methoxynaphthaleneHCID 603535—

반응 조건

온도95 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05792886
출처 데이터셋uspto-grants-1998_08
ORD IDord-ed75f97fb4d04c68b12c8d5500858c77
출처 메모uspto-grants-1998_08