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