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(4-MORPHOLIN-4-YL-PHENYL)METHANOL

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(4-MORPHOLIN-4-YL-PHENYL)METHANOL Basic information

Product Name:
(4-MORPHOLIN-4-YL-PHENYL)METHANOL
Synonyms:
  • 4-Morpholinobenzyl Alcohol
  • 4-(Morpholin-4-yl)benzyl alcohol
  • 4-(Morpholin-4-yl)benzyl alcohol, 4-[4-(Hydroxymethyl)phenyl]morpholine
  • (4-MORPHOLINOPHENYL)METHANOL
  • (4-MORPHOLIN-4-YL-PHENYL)METHANOL
  • RARECHEM AL BD 1130
  • BUTTPARK 98\50-30
  • (4-MORPHOLIN-4-YL-PHENYL)METHANOL 95%
CAS:
280556-71-0
MF:
C11H15NO2
MW:
193.24
Product Categories:
  • Alcohols and Derivatives
  • Heterocycles
Mol File:
280556-71-0.mol
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(4-MORPHOLIN-4-YL-PHENYL)METHANOL Chemical Properties

Melting point:
96 °C
Boiling point:
378.4±42.0 °C(Predicted)
Density 
1.160±0.06 g/cm3(Predicted)
storage temp. 
Storage temp. 2-8°C
form 
powder
pka
14.40±0.10(Predicted)
color 
White
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
Hazard Note 
Irritant
HS Code 
2934999090
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(4-MORPHOLIN-4-YL-PHENYL)METHANOL Usage And Synthesis

Synthesis

541-41-3

7470-38-4

280556-71-0

C. Synthesis of 4-(4-morpholinyl)benzyl alcohol. At -10 °C, 4-(4-morpholinyl)benzoic acid (1.00 g, 4.83 mmol) and 4-methylmorpholine (0.53 mL, 4.8 mmol) were dissolved in tetrahydrofuran (25 mL), followed by the addition of ethyl chloroformate (0.46 mL, 4.8 mmol). After 0.25 h of reaction, sodium borohydride (550 mg, 14.5 mmol) was added to the mixture followed by slow addition of methanol (50 mL). Next, the mixture was treated with 5% aqueous acetic acid, after which the mixture was concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to give 164 mg (18% yield) of 4-morpholinobenzyl alcohol. The product was characterized by 1H NMR, IR spectroscopy, field desorption mass spectrometry (FD-MS, m/e 193 (M+)), and elemental analysis (calculated values for C11H15NO2: C, 68.37; H, 7.82; N, 7.25; measured values: C, 68.46; H, 7.95; N, 7.21).

References

[1] Patent: US6610704, 2003, B1

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