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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22724Generated: October 25, 2026

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

https://huagongshe.com/reaction/22724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant2,4-DichlorobenzaldehydeHCID 13404—
Reactant2-Amino-4-methoxyphenolHCID 1419108—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-(2,4-Dichlorophenyl)-5-methoxybenzoxazoleHCID 21911684—

Reaction Conditions

Temperature45 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849632B2
Source datasetuspto-grants-2005_02
ORD IDord-b49a608ab03748af805287bb5e78d29f
Source noteuspto-grants-2005_02