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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | 2,4-Dichlorobenzaldehyde | HCID 13404 | — |
| Reactant | 2-Amino-4-methoxyphenol | HCID 1419108 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2,4-Dichlorophenyl)-5-methoxybenzoxazole | HCID 21911684 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06849632B2 |
|---|
| Source dataset | uspto-grants-2005_02 |
|---|
| ORD ID | ord-b49a608ab03748af805287bb5e78d29f |
|---|
| Source note | uspto-grants-2005_02 |
|---|