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162358-05-6

162358-05-6 Structure

162358-05-6 Structure
IdentificationBack Directory
[Name]

2-(4-OCTYLPHENYL)ETHANOL
[CAS]

162358-05-6
[Synonyms]

4-Octyl-benzeneethanol
Benzeneethanol, 4-octyl
2-(4-OCTYLPHENYL)ETHANOL
4-Octylphenethyl alcohol
[Molecular Formula]

C16H26O
[MDL Number]

MFCD09753531
[MOL File]

162358-05-6.mol
[Molecular Weight]

234.377
Chemical PropertiesBack Directory
[Appearance]

Oil
[Boiling point ]

306.3±10.0℃ (760 Torr)
[density ]

0.931±0.06 g/cm3 (20 ºC 760 Torr)
[Fp ]

116.2±4.2℃
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform, Ethyl Acetate, Hexane
[form ]

Oil
[pka]

14.92±0.10(Predicted)
[CAS DataBase Reference]

162358-05-6
Hazard InformationBack Directory
[Chemical Properties]

Oil
[Uses]

2-(4-Octylphenyl)ethanol (cas# 162358-05-6) is a compound useful in organic synthesis.
[Synthesis]

2-(4-Octylphenyl)ethyl acetate

162358-04-5

2-(4-OCTYLPHENYL)ETHANOL

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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-(4-OCTYLPHENYL)ETHANOL(162358-05-6)1HNMR
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