돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 563453생성일: 2026년 10월 23일

Dimethyl Sulfoxide → 1-Bromo-2-methoxynaphthalene

https://huagongshe.com/ko/reaction/563453

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Methyl iodideHCID 6328—
반응물1-Bromo-2-naphtholHCID 11316—
반응물Potassium HydroxideHCID 14797—
용매WaterHCID 962—
생성물1-Bromo-2-methoxynaphthaleneHCID 7286069%

반응 단계

A 500 mL three-necked round-bottomed flask was charged with 1-bromonaphthalen-2-ol (30.0 g, 134.5 mmol), potassium hydroxide (KOH) (11.3 g, 201.7 mmol) and DMSO (300 mL), and the mixture was stirred under nitrogen atmosphere for 10 minutes, After cooling the mixture by using ice-water bath, iodomethane (28.6 g, 201.7 mmol) was slowly added dropwise thereto. Then, the resultant mixture was stirred under nitrogen atmosphere at ambient temperature for 12 hours, and then at 50° C. for 1 hour. After cooling to ambient temperature, the reaction mixture was mixed with water (500 mL), and extracted with diethyl ether. Organic mixture was washed three times with distilled water, and dried over anhydrous magnesium sulfate (MgSO4). After removing the solvent by using a rotary evaporator, the residue was purified via silica gel column chromatography (eluent: n-hexane) to obtain 1-bromo-2-methoxynaphthalene (22.0 g, yield: 69.0%) as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067511B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-5f3bba70d52444a189792b56345d99b6
출처 메모uspto-grants-2011_11