Basic information Safety Supplier Related

m-(Methylamino)phenol

Basic information Safety Supplier Related

m-(Methylamino)phenol Basic information

Product Name:
m-(Methylamino)phenol
Synonyms:
  • m-Hydroxy-N-methylaniline
  • N-Methyl-m-aminophenol
  • N-Methyl-m-hydroxyaniline
  • 3-(Methylamino)phenol
  • m-(Methylamino)phenol
  • Phenol, 3-(methylamino)-
  • Neostigmine bromide Impurity 13
  • Neostigmine bromide Impurity G
CAS:
14703-69-6
MF:
C7H9NO
MW:
123.15
Mol File:
14703-69-6.mol
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m-(Methylamino)phenol Chemical Properties

Boiling point:
169.5 °C(Press: 12 Torr)
Density 
1.147±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Oil
pka
10.13±0.10(Predicted)
color 
Dark Beige to Dark Brown
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Safety Information

HS Code 
2922290090
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m-(Methylamino)phenol Usage And Synthesis

Synthesis

591-27-5

109-94-4

14703-69-6

Example 8A Synthesis of 3-(methylamino)phenol: 3-aminophenol (5.37 g, 49.2 mmol) was dissolved in methyl acetate (30 mL), p-toluenesulfonic acid (50 mg) was added as a catalyst, and the reaction was heated to reflux for 18 hours. Upon completion of the reaction, the volatile solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate, washed sequentially with 1N HCl, saturated NaHCO3 solution and brine, dried with Na2SO4 and filtered, and the filtrate was concentrated under reduced pressure to obtain the crude product. The crude product was dissolved in tetrahydrofuran (THF, 25 mL), 1M borane tetrahydrofuran complex (27.2 mL, 27.2 mmol) of THF solution was added and the reaction was carried out for 18 h at room temperature. At the end of the reaction, the reaction was quenched by careful addition of 1N HCl and stirred for 30 min before the reaction solution was alkalized and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over Na2SO4 and filtered and the filtrate was concentrated under reduced pressure. The residue was purified by fast chromatography (30% ethyl acetate/hexane as eluent) to afford the target compound 3-(methylamino)phenol as a viscous yellow oil (1.72 g, 28% yield). The structure of the product was confirmed by 1H NMR (300 MHz, CDCl3) and mass spectrometry (DCI/NH3): 1H NMR δ 7.03 (t, 1H), 6.13-6.24 (m, 2H), 6.11 (t, 1H), 4.54 (bs, 1H), 3.72 (bs, 1H), 2.82 (s, 3H); MS m/z 124 (M + H )+, 141 (M + NH4)+.

References

[1] Patent: US2004/19042, 2004, A1. Location in patent: Page/Page column 9-10

m-(Methylamino)phenolSupplier

Adamas Reagent, Ltd.
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Shandong Xiya Chemical Co., Ltd
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SuZhou ShiYa Biopharmaceuticals, Inc.
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Amatek Scientific Co. Ltd.
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Bide Pharmatech Ltd.
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