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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1057842생성일: 2026년 10월 26일

6-(2,6-Dimethoxyphenyl)-1,1,4,4-tetramethy-1,2,3,4-tetrahydronaphthalene → 6-(5-Bromo-2,6-dimethoxyphenyl)-1,1,4,4-tetramethy-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1057842

반응식

참여 물질

역할이름HCID투입량
반응물6-(2,6-Dimethoxyphenyl)-1,1,4,4-tetramethy-1,2,3,4-tetrahydronaphthaleneHCID 21106916—
반응물PyridiniumtribromideHCID 21124087—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물6-(5-Bromo-2,6-dimethoxyphenyl)-1,1,4,4-tetramethy-1,2,3,4-tetrahydronaphthaleneHCID 6946171157%

반응 단계

To a solution of 6-(2,6-dimethoxyphenyl)-1,1,4,4-tetramethy-1,2,3,4-tetrahydronaphthlene (340 mg, 1.05 mmol) in dichloromethane (10 mL) was added pyridinium tribromide (335 mg, 1.05 mmol) and the reaction mixture stirred at room temperature overnight. The solution was diluted with ethyl acetate and washed successively with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was purified on silica gel (eluent: ethyl acetate/hexane, 0.5:9.5) to give 0.24 g (57%) of 6-(5-bromo-2,6-dimethoxyphenyl)-1,1,4,4-tetramethy-1,2,3,4-tetrahydronaphthlene. 1H NMR (500 MHz; CDCl3): δ1.28 (s, 6H); 1.31 (s, 6H); 1.70 (s, 4H); 3.35 (s, 3H); 3.73 (s, 3H); 7.14 (dd, J1=1.5 Hz, J2=8.5 Hz, 1H); 7.15 (dd, J1=2.0 Hz, J2=8.5 Hz, 1H); 7.30 (d, J=8.0 Hz, 1H); 7.36 (d, J=1.5 Hz, 1H); 7.45 (d, J=8.0 Hz, 1H), 7.95 (br, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06515003B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-37a8c2f0d5134d33b0ac84041468c800
출처 메모uspto-grants-2003_02