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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61802생성일: 2026년 10월 25일

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 3-Bromo-9-methoxy-6,6-dimethyl-5,6-dihydro-benzo[b]carbazol-11-one

https://huagongshe.com/reaction/61802

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물Ethyl AcetateHCID 8857—
반응물3-Bromophenylhydrazine hydrochlorideHCID 33757—
반응물6-Methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2-oneHCID 12561944—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매tert-Butyl methyl etherHCID 15413—
생성물3-Bromo-9-methoxy-6,6-dimethyl-5,6-dihydro-benzo[b]carbazol-11-oneHCID 6683452046%

반응 조건

온도100 °C

반응 단계

6-Methoxy-1,1-dimethyl-3,4-dihydro-1H-naphthalen-2-one (Compound J2, 2.15 g, 10.5 mmol) and 3-bromophenylhydrazine hydrochloric acid salt (3.11 g, 1.3 eq.) were dissolved in acetic acid (12 mL), and stirred at 100° C. for 2.5 hr under nitrogen atmosphere. After cooling, the reaction solution was added with ethyl acetate, washed with water, saturated aqueous solution of sodium hydrogen carbonate, and saturated brine, and dried over magnesium sulfate. After the filtration, it was concentrated under reduced pressure. The resulting residues were dissolved in THF (30 mL) and water (3 mL), added with DDQ (5.96 g, 2.5 eq.) at 0° C., and then stirred at room temperature overnight. The reaction solution was added with MTBE, washed with 0.5 N aqueous solution of sodium hydroxide and saturated brine, and dried over magnesium sulfate. After filtration and the concentration under reduced pressure, the resulting residues were washed with MTBE to obtain the title compound (brown solid, 1.80 g, 46%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440922B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-4c3f07123dfe4df0ae246339a8f3665c
출처 메모uspto-grants-2016_09