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150712-57-5

6-Hydroxy-2-methoxynaphthalene synthesis

6synthesis methods
3900-49-0 Synthesis
2,5-Dimethoxynaphthalene

3900-49-0
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6-Hydroxy-2-methoxynaphthalene

150712-57-5
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Yield:150712-57-5 27%

Reaction Conditions:

with bromocatecholborane in 1,2-dichloro-ethane; for 72 h;Heating / reflux;

Steps:

3 EXAMPLE 3; N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-5-methoxy-2-naphthamide hydrochloride

Bromocatecholborane (4.11 g, 20.7 mmol) is added to a solution of 1,6-dimethoxynaphthalene (3.89 g, 20.7 mmol) in dichloroethane (60 mL). The resulting solution is heated to reflux for 72 hours, allowed to cool, and then poured into 1N HCl. The resulting mixture is extracted three times with CH2Cl2. The combined organic layers are dried (Na2SO4), filtered and concentrated to dryness. The product is purified by three columns (step gradient of 50-60-65%CH2Cl2 in hexanes) to give 5-methoxy-2-hydroxy naphthalene as an oil that solidifies on sitting (955 mg, 27%). 1H NMR (300 MHz, CDCl3) δ8.17, 7.2-7.4, 7.0-7.1, 6.66, 5.08, 3.97.

References:

US2003/236270,2003,A1 Location in patent:Page 38