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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895165Generated: October 30, 2026

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

https://huagongshe.com/reaction/895165

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 1 N 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 numberUS06914074B2
Source datasetuspto-grants-2005_07
ORD IDord-69e6ede2098e4c3a8c133c4ec4548fb9
Source noteuspto-grants-2005_07