ChemicalBook--->CAS DataBase List--->199328-35-3

199328-35-3

199328-35-3 Structure

199328-35-3 Structure
IdentificationBack Directory
[Name]

BENZENEACETIC ACID, 4-BROMO-2-NITRO-, ETHYL ESTER
[CAS]

199328-35-3
[Synonyms]

Ethyl 2-(4-bromo-2-nitrophenyl)
ethyl 4-bromo-2-nitrophenylacetate
2-(4-bromo-2-nitrophenyl)acetic acid ethyl ester
(4-Bromo-2-nitro-phenyl)-acetic acid ethyl ester
BENZENEACETIC ACID, 4-BROMO-2-NITRO-, ETHYL ESTER
[Molecular Formula]

C10H10BrNO4
[MDL Number]

MFCD11977365
[MOL File]

199328-35-3.mol
[Molecular Weight]

288.09
Chemical PropertiesBack Directory
[Boiling point ]

345℃
[density ]

1.542
[Fp ]

163℃
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Brown to orange Solid
Spectrum DetailBack Directory
[Spectrum Detail]

BENZENEACETIC ACID, 4-BROMO-2-NITRO-, ETHYL ESTER(199328-35-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

(4-BROMO-2-NITRO-PHENYL)-ACETIC ACID

6127-11-3

BENZENEACETIC ACID, 4-BROMO-2-NITRO-, ETHYL ESTER

199328-35-3

General procedure for the synthesis of ethyl 4-bromo-2-nitrophenylacetate from ethanol and 2-(4-bromo-2-nitrophenyl)acetic acid: to a solution of 2-(4-bromo-2-nitrophenyl)acetic acid (7.00 g, 27.0 mmol) in ethanol (60 mL) was slowly added concentrated sulfuric acid (1 mL). The reaction mixture was heated to reflux and maintained for 2 hours. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure. The concentrated residue was dissolved in ethyl acetate (250 mL) and separated by extraction with saturated sodium carbonate solution (50 mL). The organic layer was washed sequentially with saturated sodium carbonate solution (50 mL) and brine (50 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give ethyl 4-bromo-2-nitrophenylacetate (8.00 g, 98% yield) as an ester liquid.

[References]

[1] Patent: WO2005/63767, 2005, A2. Location in patent: Page/Page column 44
[2] Patent: US2007/78147, 2007, A1. Location in patent: Page/Page column 72
[3] Patent: WO2008/73480, 2008, A1. Location in patent: Page/Page column 27; 28
[4] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 2, p. 140 - 145
[5] Patent: WO2006/52936, 2006, A2. Location in patent: Page/Page column 48
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