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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 719181생성일: 2026년 10월 26일

Methyl iodide → 8-Amino-2-naphthalenol

https://huagongshe.com/reaction/719181

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물8-Amino-2-naphthalenolHCID 8358—
반응물Cleve's acidHCID 8386—
반응물Sodium hydrideHCID 24758—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물8-Amino-2-naphthalenolHCID 8358—
생성물7-Methoxynaphthalen-1-amineHCID 235817—

반응 단계

8-Amino-naphthalen-2-ol was prepared from 8-amino-2-naphthalenesulphonic acid (commercially available) according to the literature (J. Org. Chem. 1949, p351). To a solution of 8-amino-naphthalen-2-ol (8.00 g) in dry N,N-dimethylformamide (80 mL) was added sodium hydride (60% dispersion in mineral oil, 3.2 g) carefully. After stirring for 4 hours the reaction mixture was cooled in an ice bath and methyl iodide (3.13 mL) was added dropwise. The reaction mixture was then stirred at room temperature for 3 days. Water (10 mL) was then added and the volatiles were removed in vacuo. The residue was dissolved in chloroform, washed with water, dried (MgSO4) and the solvent removed in vacuo to yield a dark oil. This was purified using flash chromatography (chloroform) to yield 7-methoxy-naphthalen-1-ylamine as a dark brown liquid (2.92 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07132419B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-d39c13159e5342e598803700f91173f1
출처 메모uspto-grants-2006_11