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

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Benzene, 2-chloro-1-methoxy-3-nitro- Basic information
Product Name:Benzene, 2-chloro-1-methoxy-3-nitro-
Synonyms:Benzene, 2-chloro-1-methoxy-3-nitro-;2-Chloro-3-nitroanisole;2-Chloro-3-methoxy-1-nitrobenzene;2-chloro-1-Methoxy-3-nitro-;2-Chloro-1-methoxy-3-nitrobenzene, 95;2-Chloro-1-methoxy-3-nitrobenzene
CAS:3970-39-6
MF:C7H6ClNO3
MW:187.58
EINECS:
Product Categories:Nitro Compounds;API intermediates;Anisoles, Alkyloxy Compounds & Phenylacetates;Chlorine Compounds
Mol File:3970-39-6.mol
Benzene, 2-chloro-1-methoxy-3-nitro- Structure
Benzene, 2-chloro-1-methoxy-3-nitro- Chemical Properties
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 Information
HS Code 2909309090
MSDS Information
Benzene, 2-chloro-1-methoxy-3-nitro- Usage And Synthesis
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
Benzene, 2-chloro-1-methoxy-3-nitro- Preparation Products And Raw materials
Raw materials2-Methoxy-6-nitro-phenylamine-->2-chloro-3-nitro-phenol-->Iodomethane-->N,N-Dimethylformamide-->Cesium carbonate
Preparation Products2-Chloro-3-methoxyaniline
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