1-(2-METHOXYPHENYL)ETHANOL
1-(2-METHOXYPHENYL)ETHANOL Basic information
- Product Name:
- 1-(2-METHOXYPHENYL)ETHANOL
- Synonyms:
-
- 2-(2-METHOXYPHENYL)ETHANOL
- 2-METHOXYPHENETHYL ALCOHOL
- 2-METHOXYPHENYL METHYL CARBINOL
- 1-(2-METHOXYPHENYL)ETHANOL
- DL-2-METHOXY-ALPHA-METHYLBENZYL ALCOHOL
- ALPHA-METHYL-2-METHOXYBENZYL ALCOHOL
- 2-methoxy-benzeneethano
- Phenethyl alcohol, o-methoxy-
- CAS:
- 7417-18-7
- MF:
- C9H12O2
- MW:
- 152.19
- EINECS:
- 231-029-9
- Product Categories:
-
- Benzhydrols, Benzyl & Special Alcohols
- Alcohols
- C9 to C30
- Oxygen Compounds
- Mol File:
- 7417-18-7.mol
1-(2-METHOXYPHENYL)ETHANOL Chemical Properties
- Melting point:
- 37 °C
- Boiling point:
- 133-135 °C/10 mmHg (lit.)
- Density
- 1.076 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.54(lit.)
- Flash point:
- >230 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- clear liquid
- pka
- 14.89±0.10(Predicted)
- color
- Colorless to Light yellow
- InChI
- InChI=1S/C9H12O2/c1-11-9-5-3-2-4-8(9)6-7-10/h2-5,10H,6-7H2,1H3
- InChIKey
- XLDRDNQLEMMNNH-UHFFFAOYSA-N
- SMILES
- C1(CCO)=CC=CC=C1OC
- LogP
- 1.557 (est)
- CAS DataBase Reference
- 7417-18-7(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- HS Code
- 29094990
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
1-(2-METHOXYPHENYL)ETHANOL Usage And Synthesis
Uses
2-Methoxyphenethyl alcohol may be used in chemical synthesis.
Synthesis
7768-28-7
74-88-4
7417-18-7
Step A: To a stirred suspension of 2-(2-hydroxyethyl)phenol (5 g, 36.2 mmol) and cesium carbonate (Cs2CO3, 38.9 g, 108.7 mmol) in acetone (100 mL) was slowly added iodomethane (6.2 g, 43.4 mmol) under ice-bath conditions. The reaction mixture was stirred continuously at 0 °C for 50 min. Upon completion of the reaction, the mixture was filtered to remove insoluble salts and the filtrate was concentrated under reduced pressure by rotary evaporator. The concentrated crude product was subjected to liquid-liquid extraction with ethyl acetate (EtOAc) and water. The organic layer was separated and dried with anhydrous sodium sulfate (Na2SO4), and the dried organic layer was concentrated by filtration to give 2-(2-methoxyphenyl)ethanol (4.5 g, 29.6 mmol, 82% yield) as a yellow solid.
References
[1] Patent: WO2015/142903, 2015, A2. Location in patent: Page/Page column 96
[2] Patent: WO2015/140133, 2015, A1. Location in patent: Page/Page column 108
[3] Patent: WO2003/103653, 2003, A1. Location in patent: Page 184-185
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