ChemicalBook--->CAS DataBase List--->3970-39-6

3970-39-6

3970-39-6 Structure

3970-39-6 Structure
IdentificationBack Directory
[Name]

Benzene, 2-chloro-1-methoxy-3-nitro-
[CAS]

3970-39-6
[Synonyms]

2-Chloro-3-nitroanisole
2-chloro-1-Methoxy-3-nitro-
2-Chloro-3-methoxy-1-nitrobenzene
2-Chloro-1-methoxy-3-nitrobenzene
Benzene, 2-chloro-1-methoxy-3-nitro-
[Molecular Formula]

C7H6ClNO3
[MDL Number]

MFCD11035883
[MOL File]

3970-39-6.mol
[Molecular Weight]

187.58
Chemical PropertiesBack Directory
[Melting point ]

93-94 °C
[Boiling point ]

290.3±20.0 °C(Predicted)
[density ]

1.366±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

wooly powder
[color ]

Gold to faint tan
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2909309090
Spectrum DetailBack Directory
[Spectrum Detail]

Benzene, 2-chloro-1-methoxy-3-nitro-(3970-39-6)1HNMR
Benzene, 2-chloro-1-methoxy-3-nitro-(3970-39-6)FT-IR
Hazard InformationBack Directory
[Synthesis]

2-chloro-3-nitro-phenol

603-84-9

Iodomethane

74-88-4

Benzene, 2-chloro-1-methoxy-3-nitro-

3970-39-6

Step B: 2-chloro-3-nitrophenol (1.3 g, 7.49 mmol) was dissolved in N,N-dimethylformamide (DMF, 10 ml), to which milled cesium carbonate (2.92 g, 8.96 mmol) was added, followed by dropwise addition of iodomethane (1.4 ml, 22.5 mmol). The reaction mixture was stirred at room temperature overnight. After completion of the reaction, DMF was removed by distillation under reduced pressure, the residue was dissolved in ether (150 ml), the organic phase was washed sequentially with water (150 ml) and saturated saline (4 x 100 ml) and then dried with anhydrous magnesium sulfate. After filtering to remove the drier, the organic phase was concentrated under reduced pressure to obtain the crude 2-chloro-3-nitroanisole (1.38 g, yield 98%) as an orange solid.

[References]

[1] Patent: WO2004/103996, 2004, A1. Location in patent: Page 42-43
[2] Patent: WO2006/7700, 2006, A1. Location in patent: Page/Page column 63
[3] Patent: US2006/19905, 2006, A1. Location in patent: Page/Page column 25
[4] Patent: WO2006/85, 2006, A1. Location in patent: Page/Page column 77
[5] Chemische Berichte, 1893, vol. 26, p. 2466
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