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2-AMINO-4-CHLORO-BENZENEMETHANOL

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2-AMINO-4-CHLORO-BENZENEMETHANOL Basic information

Product Name:
2-AMINO-4-CHLORO-BENZENEMETHANOL
Synonyms:
  • 2-AMINO-4-CHLORO-BENZENEMETHANOL
  • (2-AMino-4-chloro-phenyl)-Methanol
  • 2-Amino-4-chlorobenzyl alcohol
  • Benzenemethanol, 2-amino-4-chloro-
  • 2-Amino-4-chlorobenzyl alcohol 98%
CAS:
37585-16-3
MF:
C7H8ClNO
MW:
157.6
Mol File:
37585-16-3.mol
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2-AMINO-4-CHLORO-BENZENEMETHANOL Chemical Properties

Melting point:
138-142°C
Boiling point:
324.2±27.0 °C(Predicted)
Density 
1.341±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
14.01±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-43
Safety Statements 
26-36/37
WGK Germany 
3
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2-AMINO-4-CHLORO-BENZENEMETHANOL Usage And Synthesis

Synthesis

22996-18-5

37585-16-3

General procedure for the synthesis of (2-amino-4-chlorophenyl)methanol from 4-chloro-2-nitrobenzenemethanol: 4-chloro-2-nitrobenzenemethanol (1 g, 5.33 mmol, ALDRICH) and platinum(IV) oxide (100 mg, 0.44 mmol) were suspended in ethanol (100 mL) and hydrogenated for 1 hr at room temperature and 1300 mbar hydrogen pressure. . After completion of the reaction, the suspension was filtered, the filter cake was washed with ethanol, and the filtrates were combined and concentrated to dryness to give the crude product (2-amino-4-chlorophenyl)methanol as a light orange solid. The crude product was purified by rapid chromatography on silica gel, the eluent being a gradient of dichloromethane solution of 0 to 3% methanol. The target fraction was collected and the solvent was evaporated to dryness to give the pure product (2-amino-4-chlorophenyl)methanol (0.650 g, 77% yield) as a light orange solid. NMR hydrogen spectrum (DMSO-d6) data: δ 4.34 (d, 2H), 5.06 (t, 1H), 5.20 (s, 2H), 6.51 (dd, 1H), 6.64 (d, 1H), 7.05 (d, 1H).

References

[1] Angewandte Chemie - International Edition, 2017, vol. 56, # 35, p. 10573 - 10576
[2] Angew. Chem., 2017, vol. 129, # 35, p. 10709 - 10712,4
[3] Synlett, 2017, vol. 28, # 14, p. 1724 - 1728
[4] Patent: WO2008/104754, 2008, A1. Location in patent: Page/Page column 178-179
[5] Journal of Medicinal Chemistry, 1993, vol. 36, # 22, p. 3397 - 3408

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