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ChemicalBook--->CAS DataBase List--->35942-94-0

35942-94-0

35942-94-0 Structure

35942-94-0 Structure
IdentificationBack Directory
[Name]

2-Furanethanol, 5-Methyl-
[CAS]

35942-94-0
[Synonyms]

5-methyl-2-Furanethanol
2-Furanethanol, 5-Methyl-
2-(5-methyl-2-furyl)ethanol
β-(5-Methyl-2-furyl)ethanol
2-(5-methylfuran-2-yl)ethanol
2-(5-methylfuran-2-yl)ethan-1-ol
2-Furanethanol, 5-Methyl- ISO 9001:2015 REACH
[Molecular Formula]

C7H10O2
[MDL Number]

MFCD15145904
[MOL File]

35942-94-0.mol
[Molecular Weight]

126.15
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly)
[form ]

Oil
[color ]

Clear Colorless
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

2-(5-Methylfuran-2-yl)ethanol is used in the synthetic preparation of selective androgen receptor modulators, which exhibits antagonist activity in some types of hormone-dependent tumors.
[Synthesis]

ETHYLENE OXIDE

75-21-8

2-Methylfuran

534-22-5

2-Furanethanol, 5-Methyl-

35942-94-0

At 0 °C and under nitrogen protection, n-butyllithium (83.0 mL, 133 mmol, 1.6 M hexane solution) was slowly added dropwise to a stirred solution of 2-methylfuran (10.0 mL, 111 mmol) in tetrahydrofuran (85 mL). The reaction mixture was stirred at room temperature for 4 hours and then cooled to 0°C again. Subsequently, ethylene oxide (8.30 mL, 166 mmol) was added slowly and the reaction mixture was gradually warmed to room temperature over 16 hours. Upon completion of the reaction, the reaction was quenched by the addition of saturated aqueous ammonium chloride, the organic layer was separated, and the aqueous layer was extracted with ether (2 x 250 mL). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure. Finally, purification by atmospheric pressure distillation (boiling point 170-185 °C) gave 10.1 g (80.3 mmol, 72% yield) of the target product 2-(5-methylfuran-2-yl)ethanol as a light yellow oil.

[References]

[1] Patent: WO2009/3077, 2008, A1. Location in patent: Page/Page column 66
[2] Advanced Synthesis and Catalysis, 2006, vol. 348, # 16-17, p. 2501 - 2508
[3] Tetrahedron, 2009, vol. 65, # 44, p. 9021 - 9029
[4] Patent: US2002/173445, 2002, A1
[5] Patent: US2004/77605, 2004, A1
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