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3-chloro-5-methoxyphenol

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3-chloro-5-methoxyphenol Basic information

Product Name:
3-chloro-5-methoxyphenol
Synonyms:
  • 3-Methoxy-5-chlorophenol
  • 3-Chloro-5-methoxyphenol,99%
  • Einecs 265-661-1
  • 65262-96-6
  • Phenol, 3-chloro-5-methoxy-
CAS:
65262-96-6
MF:
C7H7ClO2
MW:
158.58
EINECS:
265-661-1
Mol File:
65262-96-6.mol
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3-chloro-5-methoxyphenol Chemical Properties

Melting point:
99℃
Boiling point:
265.3±20.0 °C(Predicted)
Density 
1.280±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
8.63±0.10(Predicted)
Appearance
Light yellow to brown Solid
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Safety Information

HS Code 
2909500090
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3-chloro-5-methoxyphenol Usage And Synthesis

Uses

3-Chloro-5-methoxyphenol is a phenol derivative containing chloro and methoxy substituents on its benzene ring structure. The product can be used as a pharmaceutical intermediate.d

Synthesis

7051-16-3

65262-96-6

General procedure for the synthesis of 3-chloro-5-methoxyphenol from 1-chloro-3,5-dimethoxybenzene (Scheme No. 4, K): 1-methyl-2-pyrrolidinone (75 mL) was added to sodium methanethiol (12.32 g, 173.80 mmol) followed by 1-chloro-3,5-dimethoxybenzene (20.00 g, 115.87 mmol). The reaction mixture was heated to 140°C and maintained for 2.5 hours, followed by stirring at room temperature overnight. Upon completion of the reaction, 1-methyl-2-pyrrolidinone was removed by distillation under reduced pressure. The residue was partitioned between ethyl acetate, water and 1N hydrochloric acid. The organic layer was sequentially washed twice with 1N hydrochloric acid and once with saturated aqueous sodium chloride solution and then dried with anhydrous magnesium sulfate. The organic solvent was removed by concentration under reduced pressure to give a pale yellow solid. The solid was purified by silica gel column chromatography (400 mL silica gel, dichloromethane as eluent). The purified fraction was collected and the solvent was removed under reduced pressure to give 3-chloro-5-methoxyphenol as a yellow solid (16.62 g, 90% yield).1H NMR (300 MHz, DMSO-d6) δ 6.43 (t, J = 2.0 Hz, 1H), 6.40 (t, J = 1.9 Hz, 1H), 6.28 (t, J = 2.1 Hz, 1H), 6.28 (t, J = 2.1 Hz, 1H) 3.71 (s, 3H); MS (APCI+) m/z 159 [M+1]; Rf = 2.04 min.

References

[1] Patent: WO2007/149033, 2007, A1. Location in patent: Page/Page column 68-69
[2] Patent: WO2012/90219, 2012, A2. Location in patent: Page/Page column 91

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