5-CHLORO-3-IODO-2-METHYLANILINE
5-CHLORO-3-IODO-2-METHYLANILINE Basic information
- Product Name:
- 5-CHLORO-3-IODO-2-METHYLANILINE
- Synonyms:
-
- 5-CHLORO-3-IODO-2-METHYLANILINE
- 5-Chloro-3-iodo-2-methylbenzenamine
- Benzenamine, 5-chloro-3-iodo-2-methyl-
- CAS:
- 870606-29-4
- MF:
- C7H7ClIN
- MW:
- 267.49
- Mol File:
- 870606-29-4.mol
5-CHLORO-3-IODO-2-METHYLANILINE Chemical Properties
- Boiling point:
- 327.8±42.0 °C(Predicted)
- Density
- 1.883±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 2.43±0.10(Predicted)
5-CHLORO-3-IODO-2-METHYLANILINE Usage And Synthesis
Synthesis
294190-16-2
870606-29-4
The general procedure for the synthesis of 5-chloro-3-iodo-2-methyl-3-nitrobenzene from 5-chloro-1-iodo-2-methyl-3-nitrobenzene was as follows: 5-chloro-1-iodo-2-methyl-3-nitrobenzene (3.0 g, 10.1 mmol) was mixed with tin(II) chloride dihydrate (9.1 g, 40.4 mmol) in acetic acid (10 mL) and stirred for 1 hour at room temperature. After the reaction was completed, the reaction mixture was diluted with ether. The mixture was cooled to 0°C and 50% aqueous sodium hydroxide solution was added slowly. The lumpy white solid generated in the reaction was removed by filtration. The filtrate was concentrated and the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate, 4:1, v/v) to afford 5-chloro-3-iodo-2-methylaniline (1.81 g, 67% yield) as a light yellow solid.1H NMR (400 MHz, CDCl3) δ 7.25 (d, 1H), 6.64 (d, 1H), 3.78 (br s 2H), 2.28 (s, 3H).
References
[1] Patent: WO2005/117909, 2005, A2. Location in patent: Page/Page column 113
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