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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23861생성일: 2026년 10월 25일

Methanol → 4-Bromo-2,6-dimethoxyphenol

https://huagongshe.com/reaction/23861

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2,6-DimethoxyphenolHCID 7041—
반응물N-bromobutanimideHCID 67184—
촉매Sodium hydrideHCID 24758—
용매DichloromethaneHCID 6344—
생성물4-Bromo-2,6-dimethoxyphenolHCID 1484587663.5%

반응 조건

온도-45 °C

반응 단계

To a 2 liter flask equipped with a magnetic stirrer, thermometer, and nitrogen inlet, was added 77 g (0.5 mol) of pyrogallol 1,3-dimethyl ether. 5.8 ml of MeOH, and 750 ml of CH2Cl2. To this solution was added 126 mg (5 mmol) of NaH (95%). The solution was stirred while cooling to −45° C. with a dry-ice acetone bath. 94 g (0.53 mol) of powdered N-bromosuccinimide was added rapidly. The reaction mixture was then stirred for 1 hour at −35° C., heated to room temperature over next 30 min, and finally refluxed for 30 min. The CH2Cl2 was removed under reduced pressure and the residue solidified. The tan solid was broken up and stirred well with 1 liter of ether. This was filtered and the residue was washed well with ether. The ether was evaporated under reduced pressure to yield a tan solid. The solid was placed in a 5 liter flask with 3 liters of ligroin (bp: 90-110° C.) and heated with stirring to 80° C. The hot solution was decanted from the brown oil and the hot yellow solution was allowed to cool at room temperature for 3 hr. The white needles was filtered off and dried to yield 74 g (63%) of 17.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855657B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-ba2f9e8d31304326b8cc2767210e50e2
출처 메모uspto-grants-2005_02