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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15632생성일: 2026년 10월 25일

2,3,5,6-Tetramethylphenol → 4-Bromo-2,3,5,6-tetramethylphenol

https://huagongshe.com/reaction/15632

반응식

참여 물질

역할이름HCID투입량
반응물2,3,5,6-TetramethylphenolHCID 10694—
반응물BromineHCID 24408—
용매Acetic AcidHCID 176—
생성물4-Bromo-2,3,5,6-tetramethylphenolHCID 27865166%

반응 단계

To a suspension of 2,3,5,6-tetramethylphenol (5.10 g, 34.0 mmol) in acetic acid (90 ml) was added dropwise a solution of bromine (1.98 mL, 38.6 mmol) in acetic acid (30 mL) at room temperature, and the mixture was stirred for 5 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate, and washed successively with aqueous sodium thiosulfate solution and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The precipitated crystals were washed with petroleum ether to give the title compound (5.10 g, yield 66%) as pale-yellow crystals. The mother solution was concentrated under reduced pressure, and washed with petroleum ether to give second crop (1.38 g, yield 18%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732626B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e4ff88d21de84e5b9e54caf6a72ae839
출처 메모uspto-grants-2010_06