ChemicalBook--->CAS DataBase List--->59803-35-9

59803-35-9

59803-35-9 Structure

59803-35-9 Structure
IdentificationBack Directory
[Name]

DIETHYL 2-(2-NITROBENZYL)MALONATE
[CAS]

59803-35-9
[Synonyms]

DIETHYL 2-[(2-NITR...
DIETHYL 2-(2-NITROBENZYL)MALONATE
Diethyl (2-nitrobenzyl)propane-1,3-dioate
Diethyl 2-(2-nitrobenzyl)propane-1,3-dioate
diethyl 2-[(2-nitrophenyl)methyl]propanedioate
DIETHYL 2-(2-(HYDROXY(OXIDO)AMINO)BENZYL)MALONATE
Propanedioic acid, 2-[(2-nitrophenyl)methyl]-, 1,3-diethyl ester
[Molecular Formula]

C14H17NO6
[MDL Number]

MFCD00110674
[MOL File]

59803-35-9.mol
[Molecular Weight]

295.29
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
Safety DataBack Directory
[HS Code ]

2917191090
Hazard InformationBack Directory
[Synthesis]

2-Nitrobenzyl bromide

3958-60-9

Diethyl malonate

105-53-3

DIETHYL 2-(2-NITROBENZYL)MALONATE

59803-35-9

General procedure for the synthesis of diethyl 2-(2-nitrobenzyl)malonate from 2-nitrobenzyl bromide and diethyl malonate: Potassium carbonate (9.6 g, 0.069 mol) was added to a stirring solution of diethyl malonate (8.89 g, 0.055 mol) in dimethylformamide (50 mL) under an inert atmosphere with continuous stirring for 15 minutes. Subsequently, a solution of 1-(bromomethyl)-2-nitrobenzene (10 g, 0.046 mol) in dimethylformamide (10 mL) was slowly added to the reaction mixture. The reaction mixture was stirred at room temperature for 2 h. The progress of the reaction was monitored by thin layer chromatography (TLC) to confirm complete consumption of raw materials. Upon completion of the reaction, the mixture was diluted with water (600 mL) and extracted with ethyl acetate (3 x 250 mL). The organic phases were combined, dried with anhydrous magnesium sulfate and subsequently concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel: 100-200 mesh, eluent: 5% hexane solution of ethyl acetate) to give the final target compound diethyl 2-(2-nitrobenzyl)malonate (8.7 g, 63% yield).

[References]

[1] Patent: WO2010/127855, 2010, A1. Location in patent: Page/Page column 145
[2] Patent: WO2005/40119, 2005, A1. Location in patent: Page/Page column 48
[3] Patent: WO2005/40100, 2005, A1. Location in patent: Page/Page column 75-77
59803-35-9 suppliers list
Company Name: Yancheng KangdiSen Pharmaceutical Co., Ltd.  
Telephone: 13812573443;18052965989
Website: https://www.chemicalbook.com/ShowSupplierProductsList19142/0_EN.htm
Company Name: Zhengzhou Acme Chemical Co., Ltd.  
Telephone: 0371-0371-55629727 13323845623
Website: http://www.acmechem.cn
Company Name: Career Henan Chemica Co  
Telephone: +86-0371-86658258 +86-13203830695
Website: www.coreychem.com/
Company Name: Amel Pharmatech Corporation  
Telephone: 027-888-4366503 13986279625
Website: www.amelpharmatech.com/
Company Name: Changzhou Yinghao Technology Development Co., Ltd  
Telephone: 15151934985
Website: http://www.yingsapharm.com/
Company Name: Energy Chemical  
Telephone: 021-58432009 400-005-6266
Website: http://www.energy-chemical.com
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-6005915
Website: www.picasso-e.com/
Company Name: Beijing Solarbio Science & Tecnology Co., Ltd.  
Telephone: 010-50973130 17801761073
Website: www.solarbio.com/
Tags:59803-35-9 Related Product Information