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HRID 217582Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/217582

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DimethoxybenzeneHCID 9016—
Edukt3,3',4,4'-Tetrakis(decyloxy)-1,1'-biphenylHCID 15473749—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,4-Dimethoxy-6,7,10,11-tetrakis(decyloxy)triphenyleneHCID 5369092184%

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198096B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-e5627bed7fb743cc8452b252aec2f8dd
Quellennotizuspto-grants-2012_06