2,6-DICHLOROPHENETHYLALCOHOL
2,6-DICHLOROPHENETHYLALCOHOL Basic information
- Product Name:
- 2,6-DICHLOROPHENETHYLALCOHOL
- Synonyms:
-
- TIMTEC-BB SBB005836
- 2,6-DICHLOROPHENETHYLALCOHOL
- 2-(2,6-DICHLOROPHENYL)ETHANOL
- 2,6-Dichlorophenethyl alcohol, 96% 5GR
- 2,6-DICHLOROPHENETHYLALCOHOL 96%
- 2,6-Dichlorophenethyl alcohol,96%
- 2,6-Dichlorophenethanol
- 2,6-Dichlorobenzeneethanol
- CAS:
- 30595-79-0
- MF:
- C8H8Cl2O
- MW:
- 191.05
- Product Categories:
-
- Benzhydrols, Benzyl & Special Alcohols
- Mol File:
- 30595-79-0.mol
2,6-DICHLOROPHENETHYLALCOHOL Chemical Properties
- Melting point:
- 59-65 °C
- Boiling point:
- 152 °C / 12mmHg
- Density
- 1.2559 (rough estimate)
- refractive index
- 1.5670 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- pka
- 14.56±0.10(Predicted)
- form
- Crystalline Powder, Crystals or Flakes
- color
- White to slightly yellow
- CAS DataBase Reference
- 30595-79-0(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- HS Code
- 29062990
MSDS
- Language:English Provider:ACROS
2,6-DICHLOROPHENETHYLALCOHOL Usage And Synthesis
Chemical Properties
white to slightly yellow crystalline powder,
Synthesis
6575-24-2
30595-79-0
(vii) Synthesis of 2,6-dichlorophenylethanol: A suspension of lithium aluminum hydride (13.75 g, 365.75 mmol) was slowly added to a solution of anhydrous ether (500 mL) containing 2,6-dichlorophenylacetic acid (50 g, 243.75 mmol) through a powder charging funnel under nitrogen protection. The reaction mixture was heated to reflux and maintained for 16 hours. Upon completion of the reaction, the reaction was quenched by slow dropwise addition of a saturated aqueous solution of sodium sulfate (25 mL). The resulting slurry was stirred at room temperature for 3 hours, followed by filtration through a Brinell funnel and washing the solid residue with ether (2 x 100 mL). The ether layer filtrates were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent to give 38.6 g (85% yield) of 2,6-dichlorophenethyl alcohol as a colorless oil.
References
[1] Journal of Medicinal Chemistry, 2007, vol. 50, # 12, p. 2818 - 2841
[2] Patent: EP1087934, 2004, B1. Location in patent: Page 28
[3] Journal of Medicinal Chemistry, 1970, vol. 13, # 6, p. 1051 - 1057
[4] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 23, p. 5211 - 5217
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