Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Analytical Chemistry >  Standard >  Pharmaceutical Impurity Reference Standards >  Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate

Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate

Basic information Safety Supplier Related

Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate Basic information

Product Name:
Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate
Synonyms:
  • METHYL 6-[3-(1-ADAMANTYL)-4-METHOXYPHENYL]-2-NAPHTHOATE
  • Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate
  • Mehtyl 6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthoate
  • 6-[3-(1-Adamantyl-4-methoxyphenyl]-2-naphthatemethylester
  • Methyl6-[3-(1-adamanty)-4-methoxyphenyl]-2-naphthoate
  • Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate(Adapalene)
  • Mehtyl 6-[3-(1-adamanty)-4-methoxy
  • Adapalene Methyl Ester
CAS:
106685-41-0
MF:
C29H30O3
MW:
426.55
EINECS:
808-698-6
Product Categories:
  • Heterocycles
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • ADAPALENE
  • (intermediate of adapalene)
  • APIs Intermediate
Mol File:
106685-41-0.mol
More
Less

Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate Chemical Properties

Melting point:
223-225°C
Boiling point:
589.6±50.0 °C(Predicted)
Density 
1.185±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly)
form 
solid
color 
White to Off-White
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/38
Safety Statements 
26
HS Code 
2918992090
More
Less

Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate Usage And Synthesis

Chemical Properties

White to Off-White Solid

Uses

Adapalene intermediate

Synthesis

33626-98-1

104224-63-7

106685-41-0

General procedure for the preparation of methyl 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthalenecarboxylate (V): magnesium scraps (1.26 g, 51.85 mmol) were mixed with THF (10 mL) under nitrogen protection and stirred at room temperature. 2-(1-adamantyl)-4-bromoanisole (IV) (1.4 g, 4.36 mmol) and 1,2-dibromoethane (0.56 mL) were added, and the reaction mixture was subsequently heated to 40 °C to initiate the reaction. Then a solution of 2-(1-adamantyl)-4-bromoanisole (12.6 g, 39.25 mmol) in THF (40 mL) was slowly added dropwise under reflux conditions for 30 min. A solution of purified zinc chloride (8.4 g, 61 mmol) in THF (30 mL) was added slowly dropwise at reflux temperature over 15 minutes. After the reaction mixture was refluxed for 1 h, methyl 6-bromo-2-naphthalenecarboxylate (8.0 g, 30 mmol) was added and stirred for 10 min, followed by the addition of NiCl2ZDPPE catalyst (0.21 g). The mixture was continued to be stirred at the same temperature for 2 h. The residue was subsequently concentrated. The residue was treated with dichloromethane (100 mL) and 1N HCl (100 mL), and the dichloromethane layer was washed sequentially with 10% EDTA disodium salt solution and water, dried with anhydrous sodium sulfate, and distilled to give the crude product. The crude product was stirred in ethyl acetate (140 mL) at 70 °C for 1 h, cooled to 15 °C and kept for 1 h. The solid was collected by filtration and dried. [Yield: 9.45 g, 50% yield].

References

[1] Organic Process Research and Development, 2006, vol. 10, # 2, p. 285 - 288
[2] Patent: WO2007/125542, 2007, A2. Location in patent: Page/Page column 16
[3] Journal of Medicinal Chemistry, 1995, vol. 38, # 26, p. 4993 - 5006

Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoateSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
chenyj@titansci.com
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
XiaoGan ShenYuan ChemPharm co,ltd
Tel
15527768836
Email
1791901229@qq.com
China Langchem Inc.
Tel
0086-21-58956006