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3,4-DICHLOROPHENETHYL ALCOHOL

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3,4-DICHLOROPHENETHYL ALCOHOL Basic information

Product Name:
3,4-DICHLOROPHENETHYL ALCOHOL
Synonyms:
  • 3,4-DICHLOROPHENETHYLALCOHOL 97%
  • 3,4-Dichlorophenethyl alcohol,97%
  • 2-(3,4-DICHLOROPHENYL)ETHANOL
  • 3,4-DICHLOROPHENETHYL ALCOHOL
  • 3,4-Dichlorophenethyl alcohol, 97% 5GR
  • 3,4-Dichlorobenzeneethanol
  • 2-(3,4-dichlorophenyl)ethan-1-ol
  • 2-(3,4-Dichlorophenyl)ethanol>
CAS:
35364-79-5
MF:
C8H8Cl2O
MW:
191.05
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
Mol File:
35364-79-5.mol
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3,4-DICHLOROPHENETHYL ALCOHOL Chemical Properties

Boiling point:
165 °C / 14mmHg
Density 
1.32
refractive index 
1.562-1.568
storage temp. 
Sealed in dry,Room Temperature
solubility 
Dichloromethane, Ethyl Acetate
form 
Liquid
color 
Clear colorless
InChI
InChI=1S/C8H8Cl2O/c9-7-2-1-6(3-4-11)5-8(7)10/h1-2,5,11H,3-4H2
InChIKey
GITOMJDYNUMCOV-UHFFFAOYSA-N
SMILES
C1(CCO)=CC=C(Cl)C(Cl)=C1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
37/38-41-51-36/37/38-20/21/22
Safety Statements 
24/25-39-26-36/37/39
RIDADR 
2810
HS Code 
29062990

MSDS

  • Language:English Provider:ACROS
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3,4-DICHLOROPHENETHYL ALCOHOL Usage And Synthesis

Chemical Properties

clear colorless liquid

Uses

Intermediate in the synthesis of σ receptor ligands.

Synthesis

5807-30-7

35364-79-5

General procedure for the synthesis of 2-(3,4-dichlorophenyl)ethanol from 3,4-dichlorophenylacetic acid: 97% lithium aluminum hydride (LiAlH4, 5.54 g, 141.63 mmol) was added batchwise to an ice-bath-cooled solution of 2-(3,4-dichlorophenyl)acetic acid (19.36 g, 94.42 mmol) in tetrahydrofuran (THF, 200 mL). After the addition was completed, the reaction mixture was stirred at room temperature for 5 hours. Upon completion of the reaction, the mixture was slowly poured into ice water (150 mL) and stirring was continued for 0.5 hours. Subsequently, THF was evaporated under reduced pressure and extracted by adding dichloromethane (DCM, 200 mL). The organic layer was separated, washed with saturated saline, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/5, v/v) to afford the target compound 2-(3,4-dichlorophenyl)ethanol (17.14 g, 95% yield) as a colorless oil.

References

[1] Journal of Medicinal Chemistry, 2007, vol. 50, # 12, p. 2818 - 2841
[2] Journal of Medicinal Chemistry, 1990, vol. 33, # 11, p. 3100 - 3110
[3] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 24, p. 5420 - 5423
[4] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 3, p. 756 - 760
[5] Journal of the American Chemical Society, 1956, vol. 78, p. 5612

3,4-DICHLOROPHENETHYL ALCOHOL Preparation Products And Raw materials

Preparation Products

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