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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217582생성일: 2026년 10월 25일

1,4-Dimethoxybenzene → 1,4-Dimethoxy-6,7,10,11-tetrakis(decyloxy)triphenylene

https://huagongshe.com/reaction/217582

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DimethoxybenzeneHCID 9016—
반응물3,3',4,4'-Tetrakis(decyloxy)-1,1'-biphenylHCID 15473749—
용매DichloromethaneHCID 6344—
생성물1,4-Dimethoxy-6,7,10,11-tetrakis(decyloxy)triphenyleneHCID 5369092184%

반응 단계

Solid 3a (5.50 g, 7.06 mmol) was added to an ice cold suspension of anhydrous FeCl3 (9.16 g, 56.5 mmol) in dry CH2Cl2 (250 mL). Within 2 min 1,4-dimethoxybenzene (3.90 g, 28.2 mmol) was added to the green reaction mixture. The reaction mixture was allowed to warm slowly to room temperature and then stir for an additional 12 h. The reaction mixture was quenched with anhydrous MeOH (30 mL). The volume of the mixture was reduced to 50 mL under reduced pressure and MeOH (200 mL) was added to the resulting oil. The slightly violet product was colled on a frit and washed with MeOH. The product was further purified by column chromatography using a 50% CH2Cl2/50% hexane solvent mixture to afford 4a (RF=0.24) as a colorless solid in 84% yield (mp 69-70° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198096B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-e5627bed7fb743cc8452b252aec2f8dd
출처 메모uspto-grants-2012_06