ChemicalBook CAS DataBase List 2-Phenylphenol

2-Phenylphenol synthesis

14synthesis methods

Product Name:2-Phenylphenol
CAS Number:90-43-7
Molecular formula:C12H10O
Molecular Weight:170.21

2-Phenylphenol can be recovered from the distillation residue of the process of phenol production via sulfonation. The phenol distillation residue contains about 40% of phenyl phenol with the other components including phenol, inorganic salts, water and so on. After vacuum distillation, the mixed phenyl phenol fraction is separated out with the vacuum being 53.3-66.7kPa. The temperature, started to be cut at 65-75 ℃ to until 100 ℃ above, but should not higher than 1345 ℃. Then take advantage of the solubility difference of ortho, p-hydroxy biphenyl in the trichlorethylene, the two are separated into pure product. The mixed material (mainly 2-hydroxy biphenyl and 4-hydroxy biphenyl) is heated to be dissolved in the trichlorethylene, after cooling, first precipitate out 4-hydroxy biphenyl crystal. After centrifuge filtration, dry to obtain 4-hydroxy biphenyl. The mother liquor was washed with a sodium carbonate solution, followed by dilute alkaline to make the 2-hydroxybiphenyl salt. After standing stratification, take the upper 2-hydroxybiphenyl sodium salt for dehydration under reduced pressure, namely, sodium salt products. The 2-hydroxybiphenylsodium salt is white to light red powder, being easily soluble in water with the solubility in 100g of water being 122g. The pH value of the 2% aqueous solution is 11.1-12.2. It is also easily soluble in acetone, methanol, soluble in glycerol, but insoluble in oil. The sodium salt of 2-hydroxy biphenyl, after acidification, can lead to the formation of 2-hydroxy biphenyl with both of them being food additives.

Silane, ([1,1'-biphenyl]-2-yloxy)trimethyl-

1022-21-5
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90-43-7
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Yield:90-43-7 99%

Reaction Conditions:

with methanol;1,3-disulfonic acid imidazolium hydrogen sulfate at 20; for 0.0666667 h;Green chemistry;

Steps:

General procedure for the deprotection of trimethylsilyl ethers

General procedure: A mixture of the substrate (1 mmol), ionic liquid [Dsim]HSO4 (6.5 mg, ～0.02 mmol) in methanol (2 mL) was stirred at room temperature. After completion of the reaction (monitored by TLC), solvent was evaporated, water (1 mL) was added to the mixture, and stirred vigorously. Decantation of the mixture gave almost pure product(s). The products were characterized by comparison of their IR and NMR data. The ionic liquid was dried at 65 ?C under vacuum to remove moisture, and then reused.

References:

Shirini, Farhad;Khaligh, Nader Ghaffari;Akbari-Dadamahaleh, Somayeh [Journal of Molecular Catalysis A: Chemical,2012,vol. 365,p. 15 - 23]

4688-76-0 Synthesis

4688-76-0
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90-43-7
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References

533-58-4 Synthesis

533-58-4
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$6.00/5g

98-80-6 Synthesis

98-80-6
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90-43-7
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References

95-56-7 Synthesis

95-56-7
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100-58-3
183 suppliers
$18.00/10ml

90-43-7
308 suppliers
$10.00/5g

References

132-64-9 Synthesis

132-64-9
343 suppliers
$5.00/10g

90-43-7
308 suppliers
$10.00/5g

References

2-Phenylphenol Related Search:

Triphenylphosphine Sodium 2-biphenylate 2-Aminophenol 2,6-Diphenylphenol 2,3,4-Trihydroxybenzoic acid Biphenyl 1-Phenyl-2-nitropropene Guaiacol p-Cresol 2-Hydroxypyridine