ChemicalBook--->CAS DataBase List--->17755-10-1

17755-10-1

17755-10-1 Structure

17755-10-1 Structure
IdentificationBack Directory
[Name]

[1,1-Biphenyl]-2-ol,3-methyl-(9CI)
[CAS]

17755-10-1
[Synonyms]

3-Methylbiphenyl-2-ol
2-Methyl-6-phenylphenol
2-(3-Methylphenyl)phenol
1,1-Biphenyl]-2-ol, 3-Methyl
[1,1-Biphenyl]-2-ol,3-methyl-(9CI)
[Molecular Formula]

C13H12O
[MDL Number]

MFCD16038030
[MOL File]

17755-10-1.mol
[Molecular Weight]

184.23
Chemical PropertiesBack Directory
[Melting point ]

37.5-38.0 °C
[Boiling point ]

129 °C(Press: 5 Torr)
[density ]

1.087
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

10.338±0.10(predicted)
[Appearance]

Colorless to light yellow Liquid
Spectrum DetailBack Directory
[Spectrum Detail]

[1,1-Biphenyl]-2-ol,3-methyl-(9CI)(17755-10-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

o-Cresol

95-48-7

Mesityl(phenyl)iodonium trifluoromethanesulfonate

144930-50-7

[1,1-Biphenyl]-2-ol,3-methyl-(9CI)

17755-10-1

The general procedure for the synthesis of 3-methylbiphenyl-2-ol from o-cresol and homotrimethylphenyl(phenyl)iodonium trifluoromethanesulfonate was as follows: to a reaction tube containing [Rh(cod)Cl]2 (3.08 mg, 0.00625 mmol), tBuOLi (40.0 mg, 0.5 mmol), diaryl iodide trifluoromethanesulfonate (0.325 mmol , 1.3 equiv) and CH3CN (2.0 mL) were added to o-cresol (0.25 mmol) and P(NMe2)3 (8.16 mg, 0.05 mmol) in a reaction tube. The reaction mixture was stirred at 130 °C for 12 h under nitrogen protection. After completion of the reaction, it was cooled to room temperature and ethyl acetate (10.0 mL) and aqueous 2N hydrochloric acid (5.0 mL) were added to the mixture and stirred vigorously for 30 min. Subsequently, the aqueous phase was extracted three times with ethyl acetate, and the organic phases were combined and washed with saturated NaHCO3 solution. The organic phase was dried with anhydrous MgSO4, filtered and passed through a diatomaceous earth pad and finally concentrated under reduced pressure. The crude product was purified by fast chromatography using hexane/ethyl acetate (30:1) as eluent.

[References]

[1] Tetrahedron, 2017, vol. 73, # 26, p. 3591 - 3595
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