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1667-12-5

1667-12-5 Structure

1667-12-5 Structure
IdentificationMore
[Name]

4,4'-Bis(hydroxymethyl)biphenyl
[CAS]

1667-12-5
[Synonyms]

4,4'-BIPHENYLDIMETHANOL
4,4'-BISBENZYL ALCOHOL
4,4'-BIS(HYDROXYMETHYL)BIPHENYL
(4'-HYDROXYMETHYL-BIPHENYL-4-YL)-METHANOL
DIPHENYL-4,4'-DIMETHANOL
[1,1ˊ-biphenyl] 4,4ˊ-dimethanol
4,4''-BIS(HYDROXYMETHYL)BIPHENYL 96%(HPLC)
4,4'-Biphenyldimethanol
[Molecular Formula]

C14H14O2
[MDL Number]

MFCD00016713
[Molecular Weight]

214.26
[MOL File]

1667-12-5.mol
Chemical PropertiesBack Directory
[Melting point ]

191-192°C
[Boiling point ]

416.3±40.0 °C(Predicted)
[density ]

1.174±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

almost transparency in hot EtOH
[form ]

powder to crystal
[pka]

14.01±0.10(Predicted)
[color ]

White to Light yellow
[CAS DataBase Reference]

1667-12-5(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H304-H332
[Precautionary statements ]

P261-P271-P301+P310-P304+P340-P312-P331-P403-P501c
[Hazard Codes ]

Xi
[Risk Statements ]

41
[Safety Statements ]

26-39
[HS Code ]

2906.29.6000
Hazard InformationBack Directory
[Chemical Properties]

White crystalline powder
[Synthesis]

Biphenyl dimethyl dicarboxylate

792-74-5

4,4'-Bis(hydroxymethyl)biphenyl

1667-12-5

a) Preparation of 4,4'-bis(hydroxy-methyl)biphenyl. In a 2-liter flask equipped with a mechanical stirrer, condenser, addition funnel and heating bath, 789 mg (20.8 mmol) of LiAlH4 was dissolved in 150 ml of anhydrous THF (tetrahydrofuran). A solution of 7.5 g (27.7 mmol) of 4,4'-bis(methoxycarbonyl)biphenyl dissolved in 500 ml of anhydrous THF was heated to 50 °C under an inert atmosphere and added dropwise to the above mixture over 1 hour. After the dropwise addition, stirring was continued at 50 °C for 30 minutes. Subsequently, the reaction mixture was cooled to room temperature and 15 ml of THF/H2O (80:20) mixture was carefully added to quench the excess LiAlH4. The reaction mixture was filtered through a Septum G2 filter and the precipitate was washed with ethanol (3 x 100 ml). The filtrate and washings were combined and evaporated to dryness under vacuum in a heating bath at 40 °C. The residue was redissolved in 100 ml of hot acetone (50 °C), filtered to remove insoluble matter, dried with anhydrous Na2SO4 and evaporated again to dryness. Finally 5.74 g of 4,4'-bis(hydroxymethyl)biphenyl was obtained in 96.6% molar yield.

[References]

[1] Patent: EP469682, 1992, A1
[2] Russian Journal of Organic Chemistry, 2008, vol. 44, # 8, p. 1172 - 1179
[3] Chemical Physics Letters, 2008, vol. 460, # 4-6, p. 474 - 477
Spectrum DetailBack Directory
[Spectrum Detail]

4,4'-Bis(hydroxymethyl)biphenyl(1667-12-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

4,4'-Biphenyldimethanol,>98.0%(GC)(1667-12-5)
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