ChemicalBook--->CAS DataBase List--->51114-73-9

51114-73-9

51114-73-9 Structure

51114-73-9 Structure
IdentificationBack Directory
[Name]

5-Nitro-1-tetralone
[CAS]

51114-73-9
[Synonyms]

5-Nitro-1-tetralone
5-Nitro-α-tetralone
5-NITRO-A-TETRALONE
5-Nitro-3,4-dihydronaphthalen-1(2H)
5-Nitro-3,4-dihydro-2H-naphthalen-1-one
3,4-dihydro-5-nitronaphthalen-1(2H)-one
5-nitro-3,4-dihydronaphthalen-1(2H)-one
5-nitro-1,2,3,4-tetrahydronaphthalen-1-one
[Molecular Formula]

C10H9NO3
[MDL Number]

MFCD09751533
[MOL File]

51114-73-9.mol
[Molecular Weight]

191.183
Chemical PropertiesBack Directory
[Melting point ]

103-104 °C
[Boiling point ]

349.9±31.0 °C(Predicted)
[density ]

1.322±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to light yellow Solid
Hazard InformationBack Directory
[Synthesis Reference(s)]

Journal of Medicinal Chemistry, 19, p. 472, 1976 DOI: 10.1021/jm00226a004
[Synthesis]

4-(2-NITRO-PHENYL)-BUTYRIC ACID

67857-97-0

5-Nitro-1-tetralone

51114-73-9

The general procedure for the synthesis of 5-nitro-α-tetralone from 4-(2-nitrophenyl)butyric acid was as follows: first, 1 g of 4-(2-nitrophenyl)butyric acid (NPBS, 4.78 mmol) and 18 g of trifluoromethanesulfonic acid (TFMS) were added to a 100 mL two-necked flask fitted with a reflux condenser and magnetic stirrer at 20 °C. Under stirring, the reaction mixture was placed in an oil bath preheated to 130 °C and stirred continuously at this temperature for 45 min. Upon completion of the reaction, the mixture was cooled and transferred to a microdistillation unit. Most of the excess TFMS was removed by distillation at 52 °C and 0.5 mbar.After distillation, the bottom residue contained 0.914 g of 5-nitro-3,4-dihydro-1(2H)-naphthalenone and 3.44 g of TFMS (as determined by the GC-ISTD/internal standard method) in 99.3% yield, with 100% conversion to NPBS and 99.3% selectivity.

[References]

[1] Patent: EP1369412, 2003, A1. Location in patent: Page 6
[2] Patent: EP1369412, 2003, A1. Location in patent: Page 6
[3] Patent: US2003/176722, 2003, A1
Spectrum DetailBack Directory
[Spectrum Detail]

5-Nitro-1-tetralone(51114-73-9)1HNMR
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