午夜插插,噜噜噜影院,啪啪伊人网,欧美熟夫,景甜吻戏视频,男人强操性感蕾丝美女视频在线网站,日本美女跳舞视频

Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

150712-57-5

6-Hydroxy-2-methoxynaphthalene synthesis

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

3900-49-0
205 suppliers
$10.00/1g

6-Hydroxy-2-methoxynaphthalene

150712-57-5
7 suppliers
inquiry

-

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