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HRID 22724Erstellt: 24. Oktober 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 2-(2,4-Dichlorophenyl)-5-methoxybenzoxazole

https://huagongshe.com/de/reaction/22724

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Edukt2,4-DichlorobenzaldehydeHCID 13404—
Edukt2-Amino-4-methoxyphenolHCID 1419108—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(2,4-Dichlorophenyl)-5-methoxybenzoxazoleHCID 21911684—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To a solution of 2-amino-4-methoxyphenol (1 g, 7.1 mmol), a compound of formula (d) in 20 mL MeOH was added 2,4-dichlorobenzaldehyde (1.2 g, 7.1 mmol), a compound of formula (e). The mixture was heated at 45° C. for 12 hours. The mixture was concentrated under reduced pressure and the residue was dissolved in 50 mL dichloromethane. To the solution was added DDQ (1.7 g, 7.8 mmol), and the mixture was allowed to stir at room temperature for 30 minutes. The reaction mixture was then diluted with an additional 30 mL of dichloromethane and washed sequentially with saturated NaHCO3 (2×50 mL) and brine. The organic layer was separated, dried over MgSO4 and concentrated under reduced pressure to yield 2-(2,4-dichlorophenyl)-5-methoxybenzoxazole, a compound of formula (f), which was purified using flash column chromatography.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06849632B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-b49a608ab03748af805287bb5e78d29f
Quellennotizuspto-grants-2005_02