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4101-32-0

4101-32-0 Structure

4101-32-0 Structure
IdentificationBack Directory
[Name]

1-(4,5-DIMETHOXY-2-NITRO-PHENYL)-ETHANONE
[CAS]

4101-32-0
[Synonyms]

1-(4,5-Dimethoxy-2-nitrophenyL
3,4-Dimethoxy-2-nitroacetophenone
2'-NITRO-4',5'-DIMETHOXYACETOPHENONE
3',4'-DIMETHOXY-6'-NITROACETOPHENONE
4',5'-Dimethoxy-2'-nitroacetophenone
1-(4,5-DIMETHOXY-2-NITRO-PHENYL)-ETHANONE
Ethanone, 1-(4,5-dimethoxy-2-nitrophenyl)-
1-(4,5-dimethoxy-2-nitrophenyl)ethan-1-one
[Molecular Formula]

C10H11NO5
[MDL Number]

MFCD00130048
[MOL File]

4101-32-0.mol
[Molecular Weight]

225.2
Chemical PropertiesBack Directory
[Melting point ]

133.5-135 °C
[Boiling point ]

389.2±37.0 °C(Predicted)
[density ]

1.245±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[color ]

Light orange to Yellow to Green
[InChI]

InChI=1S/C10H11NO5/c1-6(12)7-4-9(15-2)10(16-3)5-8(7)11(13)14/h4-5H,1-3H3
[InChIKey]

ZVLFGESHYMKNQP-UHFFFAOYSA-N
[SMILES]

C(=O)(C1=CC(OC)=C(OC)C=C1[N+]([O-])=O)C
[EPA Substance Registry System]

Ethanone, 1-(4,5-dimethoxy-2-nitrophenyl)- (4101-32-0)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)
GHS02
[Signal word ]

Warning
[Hazard statements ]

H226
[Precautionary statements ]

P501-P240-P210-P233-P243-P241-P242-P280-P370+P378-P303+P361+P353-P403+P235
[HS Code ]

2913.00.4000
Hazard InformationBack Directory
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 55, p. 1585, 1990 DOI: 10.1021/jo00292a038
[Synthesis]

3,4-Dimethoxyacetophenone

1131-62-0

1-(4,5-DIMETHOXY-2-NITRO-PHENYL)-ETHANONE

4101-32-0

General procedure for the synthesis of 1-(4,5-dimethoxy-2-nitrophenyl)ethanone from 3,4-dimethoxyacetophenone: (1) Nitration step: a solution was prepared by dissolving 3,4-dimethoxyacetophenone (1,500 g) in 17% nitric acid (1,400 g) at 5 to 10 °C, followed by slow dropwise addition to a solution consisting of 67% nitric acid (8430 g) and sodium nitrite (18 g) (18 g). The titration process was controlled to be completed within 2 to 3 hours. After the dropwise addition, the reaction solution was continued to be stirred at 5 to 10°C for 1 to 2 hours. Cold water (7.5 L) was added to dilute the reaction mixture and stirred for 30 minutes. The reaction mixture was filtered and the filter cake was washed with water (30 L). The solid product obtained by filtration was re-suspended in water (7.5 L), neutralized with aqueous sodium bicarbonate to pH neutral, filtered again and washed with water (7 L). Finally, the product was dried under reduced pressure to afford 3,4-dimethoxy-6-nitroacetophenone (2164 g, 87.9% yield). The structure of the product was confirmed by 1H-NMR (400 MHz, CDCl3): δ 2.50 (s, 3H), 3.97 (s, 3H), 3.99 (s, 3H), 6.76 (s, 1H), 7.62 (s, 1H).

[References]

[1] Patent: EP1559715, 2005, A1. Location in patent: Page/Page column 17
[2] Heterocycles, 2016, vol. 92, # 10, p. 1882 - 1887
[3] Chemistry Letters, 2000, # 7, p. 712 - 713
[4] Patent: EP3205650, 2017, A1. Location in patent: Paragraph 0106; 0354; 0355
[5] Journal of Organic Chemistry, 1999, vol. 64, # 21, p. 7988 - 7995
Spectrum DetailBack Directory
[Spectrum Detail]

1-(4,5-DIMETHOXY-2-NITRO-PHENYL)-ETHANONE(4101-32-0)1HNMR
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