ChemicalBook--->CAS DataBase List--->153775-42-9

153775-42-9

153775-42-9 Structure

153775-42-9 Structure
IdentificationBack Directory
[Name]

4-cyano-3-nitrobenzoic acid
[CAS]

153775-42-9
[Synonyms]

4-cyano-3-nitrobenzoic acid
Benzoic acid, 4-cyano-3-nitro-
[Molecular Formula]

C8H4N2O4
[MDL Number]

MFCD16876894
[MOL File]

153775-42-9.mol
[Molecular Weight]

192.13
Chemical PropertiesBack Directory
[Melting point ]

205-206 °C
[Boiling point ]

438.1±40.0 °C(Predicted)
[density ]

1.56±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

2.91±0.10(Predicted)
[color ]

Pale Yellow to Light Yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
Spectrum DetailBack Directory
[Spectrum Detail]

4-cyano-3-nitrobenzoic acid(153775-42-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Methyl-2-nitrobenzonitrile

26830-95-5

4-cyano-3-nitrobenzoic acid

153775-42-9

Example 17: Alternative preparation of 4-cyano-3-nitrobenzoic acid Periodic acid (492 g, 2.17 mol) was dissolved in acetonitrile (7.71 L) under an inert atmosphere with vigorous stirring. after 15 min, chromium (VI) oxide (25 g, 0.25 mol) and 4-methyl-2-nitrobenzonitrile (100 g, 0.62 mol) were added sequentially. The reaction mixture was stirred at room temperature for 16 hours. The reaction mixture was decanted and the supernatant was filtered. The filtrate was concentrated and the residue was partitioned between 1 M aqueous sodium carbonate solution and dichloromethane. The precipitate was separated by filtration to give 4-cyano-3-nitrobenzoic acid (150 g). The filtrate was extracted twice with dichloromethane and then acidified with aqueous 4N hydrochloric acid to pH 1. The acidified filtrate was extracted three times with dichloromethane. The organic extracts were combined, dried over sodium sulfate and concentrated. The residue was partitioned between 1 M aqueous sodium carbonate and dichloromethane. The precipitate was separated by filtration to give 4-cyano-3-nitrobenzoic acid (26.67 g). Total yield: 150 g + 26.67 g = 176.67 g; 74.5% yield.

[References]

[1] Patent: WO2008/74427, 2008, A1. Location in patent: Page/Page column 52
[2] Patent: WO2012/59442, 2012, A2. Location in patent: Page/Page column 88-89
[3] Journal of Medicinal Chemistry, 2018, vol. 61, # 24, p. 11250 - 11260
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