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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 563454생성일: 2026년 10월 25일

Ammonium Chloride → 2-Methoxy-1-phenylnaphthalene

https://huagongshe.com/reaction/563454

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

In 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), mixture of water (60 mL) and dimethoxyethane (120 mL) was added, and the resultant mixture was heated under reflux for 6 hours. After cooling to ambient temperature, aqueous ammonium chloride (150 mL) and diethyl ether (200 mL) were charged thereto. The organic layer was isolated, and the residue was extracted with diethyl ether. Combined organic layer was dried over magnesium sulfate, and evaporated to remove the volatiles. Purification via silica gel column chromatography (eluent: hexane) gave 2-methoxy-1-phenylnaphthalene (13.0 g, yield: 66%) as colorless liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067511B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-478e6e1c71fe4c42a26002ea40ca122f
출처 메모uspto-grants-2011_11