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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830614Generated: November 1, 2026

2-Methoxy-7-(4-methoxyphenyl)naphthalene → 7-(4-Hydroxyphenyl)-2-naphthol

https://huagongshe.com/reaction/1830614

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-7-(4-methoxyphenyl)naphthaleneHCID 11737149—
ReactantPyridinium hydrochlorideHCID 21584435—
SolventHydrochloric AcidHCID 313—
Product7-(4-Hydroxyphenyl)-2-naphtholHCID 1017140939.5%

Reaction Conditions

Temperature190 °C

Reaction Steps

2-Methoxy-7-(4-methoxy-phenyl)naphthalene (1.02 g, 3.86 mmol) was added to of pyridinium HCl (10 g) at 190° C. The solution was stirred for 3 hr at 190° C. and cooled to room temperature and stirred with 200 mL of 1N HCl. The resulting suspension was filtered and dissolved ethyl acetate (500 mL). The combined organic layers were washed with water (200 mL), dried over magnesium sulfate, filtered, the solvent removed under vacuum, and the product purified by silica chromatography (40% ethyl acetate-hexanes to yield 0.36 g (39%) of a white solid: mp 210° C.; 1H NMR (DMSO-d6): δ 6.89 (2H, d, J=8.58 Hz), 7.05 (1H, dd, J=2.42 Hz, J=8.77 Hz), 7.17 (1H, d, J=2.24 Hz), 7.52 (1H, dd, J=1.68 Hz, J=8.40 Hz), 7.61. (2H, d, J=8.58 Hz), 7.74 (1H, d, J=8.58 Hz), 7.79 (1H, d, J=8.58 Hz), 7.86 (1H, d, J=1.12 Hz), 9.60 (1H, bs), 9.72 (1H, bs); MS (ESI) m/z 235 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067524B2
Source datasetuspto-grants-2006_06
ORD IDord-f601d44584ef495185ef7dc45327efb9
Source noteuspto-grants-2006_06