![](/CAS/GIF/601-88-7.gif)
2,6-Dichloronitrobenzene synthesis
- Product Name:2,6-Dichloronitrobenzene
- CAS Number:601-88-7
- Molecular formula:C6H3Cl2NO2
- Molecular Weight:192
![2,6-Dichloroaniline](/CAS/GIF/608-31-1.gif)
608-31-1
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$12.00/25g
![2,6-Dichloronitrobenzene](/CAS/GIF/601-88-7.gif)
601-88-7
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$8.00/5g
Yield:601-88-7 92%
Reaction Conditions:
Stage #1:2,6-Dichloroaniline with sodium tungstate (VI) dihydrate;sulfuric acid in methanol at 40;
Stage #2: with dihydrogen peroxide in methanol;water; pH=0.5 at 40; for 9 h;
Stage #3: with potassium hydroxide in methanol;water at 20 - 40; for 2 h;Reagent/catalyst;pH-value;Temperature;Solvent;
Steps:
1 Example 1 Production of 2,6-Dichloronitrobenzene
1.32 g (4.0 mmol) of sodium tungstate dihydrate and 4.0 g (40 mmol) of concentrated sulfuric acid were added to a solution of 16.2 g (100 mmol) of 2,6-dichloroaniline in 120 ml of methanol, and the mixture was heated to 40° C. 30 ml (291 mmol) of a 30% hydrogen peroxide solution was added dropwise over 10 hours.
The pH value at this time was 0.5.
After the completion of the dropwise addition, the mixture was stirred at 40° C. for 9 hours.
After the disappearance of the 2,6-dichloroaniline was confirmed by gas chromatography (area percentage method), a solution of 9.8 g (150 mmol) of 86% potassium hydroxide in 24.3 ml of methanol was added dropwise while the temperature of the reaction liquid was adjusted to 40° C. or less.
After the completion of the dropwise addition, the mixture was stirred at room temperature for 2 hours, and the reaction was completed.
After the completion of the reaction, 95 ml of toluene and 32 ml of water were added, and the mixture was stirred for a while, and filtered.
The filtrate was separated.
The obtained organic phase was washed with 8 ml of water, and then heated to reflux, and dehydrated.
Thus, 2,6-dichloronitrobenzene was obtained as a toluene solution.
This solution was analyzed by gas chromatography by the absolute calibration method, and as a result, the yield was 92%.
References:
IHARA CHEMICAL INDUSTRY CO., LTD.;Tani, Shinki;Yadomatsu, Nami;Ikumi, Akiko;Hirano, Yuuki;Ido, Takuya US2014/163256, 2014, A1 Location in patent:Paragraph 0161-0162
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