bis(3-Methoxyphenyl)aMine CAS 92248-06-1

Introduction:Basic information about bis(3-Methoxyphenyl)aMine CAS 92248-06-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

bis(3-Methoxyphenyl)aMine Basic information

Product Name:bis(3-Methoxyphenyl)aMine
Synonyms:bis(3-Methoxyphenyl)aMine;Benzenamine, 3-methoxy-N-(3-methoxyphenyl)-;3-Methoxy-N-(3-methoxyphenyl)aniline;bis(3-Methoxyphenyl)aMine ISO 9001:2015 REACH
CAS:92248-06-1
MF:C14H15NO2
MW:229.27
EINECS:
Product Categories:
Mol File:92248-06-1.mol

bis(3-Methoxyphenyl)aMine Chemical Properties

Boiling point 175-178 °C(Press: 0.8 Torr)
density 1.126±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka0.14±0.50(Predicted)

Safety Information

bis(3-Methoxyphenyl)aMine Usage And Synthesis

Synthesis

10365-98-7

536-90-3

92248-06-1

General procedure for the synthesis of bis(3-methoxyphenyl)amines from 3-methoxyphenylboronic acid and m-aminoanisole:1. copper acetate (2.1 mmol) and pyridine (0.25 mL) were added to a vigorously stirred solution of anhydrous dichloromethane (3.5 mL) of 3-methoxyaniline (1 mmol) and 3-methoxyphenylboronic acid (2 mmol) under nitrogen protection.2. The reaction mixture was stirred at room temperature for 72 hours, during which time the progress of the reaction was monitored by thin layer chromatography (TLC).3. Upon completion of the reaction, the crude reaction mixture was pre-adsorbed onto silica gel and the target product, bis(3-methoxyphenyl)amine (3c), was subsequently isolated by fast column chromatography.4. Product yield: 25%; EI-MS m/z: 229 (M+) [Ref: Urgaonkar, S.; Verkade, J.G. J. Org. Chem. 2004, 69, 9135-9142].

References[1] Patent: WO2007/79593, 2007, A1. Location in patent: Page/Page column 31

bis(3-Methoxyphenyl)aMine Preparation Products And Raw materials

Raw materials3-Methoxyphenylboronic acid-->Phenol, 3-[(3-methoxyphenyl)amino]--->3-Bromoanisole-->Iodomethane-->m-Anisidine-->N,N,N',N'-Tetramethylethylenediamine-->Pyridine-->Dichloromethane
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