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HRID 217582作成日:2026年10月26日

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

https://huagongshe.com/reaction/217582

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DimethoxybenzeneHCID 9016—
反応物3,3',4,4'-Tetrakis(decyloxy)-1,1'-biphenylHCID 15473749—
溶媒DichloromethaneHCID 6344—
生成物1,4-Dimethoxy-6,7,10,11-tetrakis(decyloxy)triphenyleneHCID 5369092184%

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198096B2
出典データセットuspto-grants-2012_06
ORD IDord-e5627bed7fb743cc8452b252aec2f8dd
出典メモuspto-grants-2012_06