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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376520Generated: October 30, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → [6-Methoxy-2-(3-methoxyphenyl)-1-naphthalenyl](4-methoxyphenyl)methanone

https://huagongshe.com/reaction/376520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant[2-(3-Methoxyphenyl)-3,4-dihydro-6-methoxynaphthalen-1-yl][4-methoxyphenyl]methanoneHCID 15434589—
Solvent1,4-DioxaneHCID 31275—
Product[6-Methoxy-2-(3-methoxyphenyl)-1-naphthalenyl](4-methoxyphenyl)methanoneHCID 1818264394%

Reaction Steps

A solution of [3,4-dihydro-6-methoxy-2-(3-methoxyphenyl)-1-naphthalenyl](4-methoxyphenyl)methanone (14.0 g, 35.0 mmol) was dissolved in anhydrous dioxane (400 mL) under an atmosphere of nitrogen. 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ, 7.0 g, 31 mmol) was added and the solution was refluxed for 16 hours. The reaction mixture was allowed to cool to ambient temperature and the solid dihydroquinone byproduct (8.8 gm) was removed by filtration and discarded. The filtrate was concentrated to dryness and the residue was purified by silica gel chromatography with chloroform as the isocratic elution solvent. Appropriate fractions gave 13.1 g, (94%) of the desired product as an oil. Although the oil contained some minor impurities, it was used without additional purification. 1H NMR (CDCl3) δ 7.88 (d, J=8.6 Hz, 1H), 7.71-7.54 (m, 4H), 7.21 (d, J=2.6 Hz, 1H), 7.18-7.05 (m, 2H), 6.99-6.89 (m, 2H), 6.78-6.70 (m, 3H), 3.94 (s, 3H), 3.78 (s,3H), 3.69 (s,3H); MS (FD) m/e 398 (M+); Anal. Calcd. for C26H22O4 : C, 78.37; H, 5.57. Found: C, 78.22; H, 5.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020513
Source datasetuspto-grants-2000_02
ORD IDord-8082e081790c4baf9bddc12331fffe21
Source noteuspto-grants-2000_02