N-[(4-methoxyphenyl)methyl]formamide

N-[(4-methoxyphenyl)methyl]formamide Suppliers list
Company Name: Yancheng KangdiSen Pharmaceutical Co., Ltd.  
Tel: 13812573443;18052965989
Email: tongbenwan22@163.com
Company Name: Tianjin Kailiqi Biotechnology Co., Ltd.  
Tel: 15076683720
Email: klq@cw-bio.com
Company Name: Aikon International Limited  
Tel: 025-58859352 13913916777
Email: dt3@aikonchem.com
Company Name: SHANGHAI FDC-CHEMICAL CO.,LTD  
Tel: 021-61469567 13774476675
Email: sales@fdc-chemical.com
Company Name: Tianjin heowns Biochemical Technology Co., Ltd.  
Tel: 400-6387771-6039 18920764717
Email: sales@heowns.com
N-[(4-methoxyphenyl)methyl]formamide Basic information
Product Name:N-[(4-methoxyphenyl)methyl]formamide
Synonyms:N-[(4-methoxyphenyl)methyl]formamide;N-(4-Methoxybenzyl)formamide;(4-methoxybenzyl)formamide;formamide, N-[(4-methoxyphenyl)methyl]-;N-[(4-methoxyphenyl)methyl]carboxamide
CAS:17061-63-1
MF:C9H11NO2
MW:165.19
EINECS:
Product Categories:
Mol File:17061-63-1.mol
N-[(4-methoxyphenyl)methyl]formamide Structure
N-[(4-methoxyphenyl)methyl]formamide Chemical Properties
storage temp. Sealed in dry,Room Temperature
Safety Information
MSDS Information
N-[(4-methoxyphenyl)methyl]formamide Usage And Synthesis
Synthesis
formamide

77287-34-4

4-Methoxybenzylamine

2393-23-9

N-[(4-methoxyphenyl)methyl]formamide

17061-63-1

The general procedure for the synthesis of N-(4-methoxybenzyl)formamide by 1,4-dioxane-mediated microwave-assisted transamidation reaction using the compound (CAS:77287-34-4) and 4-methoxybenzylamine as raw materials was as follows: to a 10 mL microwave reaction vial, which was pre-oven-dried and fitted with a Teflon-coated magnetic stirring bar, were added sequentially formamide (1 mmol), 4- methoxybenzylamine (1 mmol) and undried 1,4-dioxane (2 mL). The reaction vial was sealed with a plastic microwave septum and stirred for 5 min at room temperature, then placed in the microwave reaction chamber and the reaction was carried out at the specified temperature and time. Upon completion of the reaction (monitored by TLC), the reaction mixture was cooled to room temperature, diluted by adding distilled water (10 mL) and subsequently extracted with ethyl acetate (3 x 10 mL). The organic phases were combined, dried with anhydrous Na2SO4, filtered and the filtrate was concentrated by rotary evaporator. The crude product was purified by column chromatography, and the eluent was a mixed solvent of ethyl acetate/hexane (10-20% volume fraction of ethyl acetate, adjusted according to the polarity of the product).

References[1] Chemical Communications (Cambridge, United Kingdom), 2012, vol. 48, # 95, p. 11626 - 11628,3
[2] Chemical Communications, 2012, vol. 48, # 95, p. 11626 - 11628
[3] Tetrahedron Letters, 2013, vol. 54, # 20, p. 2553 - 2555
[4] RSC Advances, 2016, vol. 6, # 58, p. 52724 - 52728
[5] Journal of Molecular Catalysis A: Chemical, 2015, vol. 403, p. 15 - 26
N-[(4-methoxyphenyl)methyl]formamide Preparation Products And Raw materials
Raw materialsANISYL FORMATE-->4-Methoxybenzyl alcohol-->formamide-->4-Methoxybenzylamine-->Ethyl formate
Preparation Products2-(4-Methoxy-phenyl)-1-methyl-pyrrolidine
Tag:N-[(4-methoxyphenyl)methyl]formamide(17061-63-1) Related Product Information
tert-butyl 4-methoxybenzylcarbamate N-(4-Methoxybenzyl)-N-methylamine N-(4-Methoxybenzyl)urea 4-Methoxybenzylamine benzyl (4-methoxybenzyl)carbamate Acetamide, 2,2,2-trifluoro-N-[(4-methoxyphenyl)methyl]-