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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245364Generated: October 25, 2026

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

https://huagongshe.com/reaction/1245364

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 (j) in 20 mL MeOH was added (2,4-dichlorophenyl)formaldehyde (1.2 g, 7.1 mmol), a compound of formula (k). 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 (1), which was purified using flash column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125876B2
Source datasetuspto-grants-2006_10
ORD IDord-3580df681d8242cf8b3e4abb1f0a8665
Source noteuspto-grants-2006_10