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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 387490생성일: 2026년 10월 24일

Ammonium Chloride → 2-Methoxy-1-phenylnaphthalene

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

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Phenylboronic AcidHCID 66827—
반응물1-Bromo-2-methoxynaphthaleneHCID 72860—
촉매TriphenylphosphineHCID 11776—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-Methoxy-1-phenylnaphthaleneHCID 1132226666%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372996B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-36571d0ab94e4cce8539905db4773d03
출처 메모uspto-grants-2013_02