2-(4-OCTYLPHENYL)ETHANOL
2-(4-OCTYLPHENYL)ETHANOL Basic information
- Product Name:
- 2-(4-OCTYLPHENYL)ETHANOL
- Synonyms:
-
- 2-(4-OCTYLPHENYL)ETHANOL
- Benzeneethanol, 4-octyl
- 4-Octyl-benzeneethanol
- 4-Octylphenethyl alcohol
- Fingolimod Impurity 46
- 2-(4-octylphenyl)ethan-1-ol
- 2-(4-0CTYLPHENYL)ETHANOL
- CAS:
- 162358-05-6
- MF:
- C16H26O
- MW:
- 234.38
- Product Categories:
-
- Aromatics Compounds
- Aromatics
- Mol File:
- Mol File
2-(4-OCTYLPHENYL)ETHANOL Chemical Properties
- Boiling point:
- 306.3±10.0℃ (760 Torr)
- Density
- 0.931±0.06 g/cm3 (20 ºC 760 Torr)
- Flash point:
- 116.2±4.2℃
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform, Ethyl Acetate, Hexane
- form
- Oil
- pka
- 14.92±0.10(Predicted)
- Appearance
- White to off-white Solid
- CAS DataBase Reference
- 162358-05-6
2-(4-OCTYLPHENYL)ETHANOL Usage And Synthesis
Chemical Properties
Oil
Uses
2-(4-Octylphenyl)ethanol (cas# 162358-05-6) is a compound useful in organic synthesis.
Synthesis
162358-04-5
162358-05-6
The general procedure for the synthesis of 4-dodecylphenylethanol from ethyl-[2-(4-octylphenyl)]acetate was as follows: sodium methanol (195 mg, 3.61 mmol) was added to a methanol (MeOH, 10 mL) solution of ethyl 4-octylphenylacetate (500 mg, 1.81 mmol). The reaction mixture was heated to reflux for 6 hours. Upon completion of the reaction, the solvent was evaporated and the residue was partitioned between ethyl acetate (EtOAc) and water. The organic layer was separated and washed with saturated saline (brine). The organic phase was dried with anhydrous sodium sulfate (Na2SO4), filtered and the solvent was evaporated to give 4-octylphenethyl alcohol (390 mg, 92% yield) as a yellow oil. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 0.88 (t, J = 6.8 Hz, 3H), 1.22-1.30 (m, 10H), 1.55-1.63 (m, 2H), 2.57 (t, J = 7.8 Hz, 2H), 2.83 (t, J = 6.6 Hz, 2H), 3.84 (t, J = 6.6 Hz , 2H), 7.11 (s, 4H).
References
[1] Journal of Organic Chemistry, 2004, vol. 69, # 11, p. 3950 - 3952
[2] Chemical Communications, 2013, vol. 49, # 21, p. 2136 - 2138
[3] Patent: WO2014/118556, 2014, A2. Location in patent: Page/Page column 50
[4] Journal of Medicinal Chemistry, 2000, vol. 43, # 15, p. 2946 - 2961
[5] Patent: US2014/235895, 2014, A1. Location in patent: Paragraph 0253
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