Synthetises of antioxidant 4,4′-furylidene bisphenol

S. E. Hao; C. Jin; H. J. Zhang

Synthetises of antioxidant 4,4′-furylidene bisphenol

S. E. Hao^*
, C. Jin
, H. J. Zhang

^*Corresponding author for this work

School of Chemistry and Chemical Engineering

Harbin Institute of Technology

Research output: Contribution to journal › Article › peer-review

Abstract

The synthetic method of 4,4′-furylidene bisphenol with phenol and furfural as raw materials and H₂SO₄, H₃PO₄, KOH, N(C₂H₅)₃ as catalysts was studied. The results showed that the yield of 4,4′-furylidene bisphenol reached 57.9% when the reaction proceeded for 3 h at 80 °C with isobutanol as solvent, N(C₂H₅)₃ as catalyst and n (phenol) : n(N(C₂H₅)₃) = 1.00:0.05. The antioxygenic activity of 4,4′-furylidene bisphenol was better than that of bisphenol A and BHT as determined by experiments.

Original language	English
Pages (from-to)	225-227
Number of pages	3
Journal	Jingxi Huagong/Fine Chemicals
Volume	18
Issue number	4
State	Published - Apr 2001

Keywords

4,4′-Furylidene bisphenol
Antioxidant
Basic catalysis

Cite this

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title = "Synthetises of antioxidant 4,4′-furylidene bisphenol",

abstract = "The synthetic method of 4,4′-furylidene bisphenol with phenol and furfural as raw materials and H2SO4, H3PO4, KOH, N(C2H5)3 as catalysts was studied. The results showed that the yield of 4,4′-furylidene bisphenol reached 57.9\% when the reaction proceeded for 3 h at 80 °C with isobutanol as solvent, N(C2H5)3 as catalyst and n (phenol) : n(N(C2H5)3) = 1.00:0.05. The antioxygenic activity of 4,4′-furylidene bisphenol was better than that of bisphenol A and BHT as determined by experiments.",

keywords = "4,4′-Furylidene bisphenol, Antioxidant, Basic catalysis",

author = "Hao, \{S. E.\} and C. Jin and Zhang, \{H. J.\}",

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TY - JOUR

T1 - Synthetises of antioxidant 4,4′-furylidene bisphenol

AU - Hao, S. E.

AU - Jin, C.

AU - Zhang, H. J.

PY - 2001/4

Y1 - 2001/4

N2 - The synthetic method of 4,4′-furylidene bisphenol with phenol and furfural as raw materials and H2SO4, H3PO4, KOH, N(C2H5)3 as catalysts was studied. The results showed that the yield of 4,4′-furylidene bisphenol reached 57.9% when the reaction proceeded for 3 h at 80 °C with isobutanol as solvent, N(C2H5)3 as catalyst and n (phenol) : n(N(C2H5)3) = 1.00:0.05. The antioxygenic activity of 4,4′-furylidene bisphenol was better than that of bisphenol A and BHT as determined by experiments.

AB - The synthetic method of 4,4′-furylidene bisphenol with phenol and furfural as raw materials and H2SO4, H3PO4, KOH, N(C2H5)3 as catalysts was studied. The results showed that the yield of 4,4′-furylidene bisphenol reached 57.9% when the reaction proceeded for 3 h at 80 °C with isobutanol as solvent, N(C2H5)3 as catalyst and n (phenol) : n(N(C2H5)3) = 1.00:0.05. The antioxygenic activity of 4,4′-furylidene bisphenol was better than that of bisphenol A and BHT as determined by experiments.

KW - 4,4′-Furylidene bisphenol

KW - Antioxidant

KW - Basic catalysis

UR - https://www.scopus.com/pages/publications/0035308453

M3 - 文章

AN - SCOPUS:0035308453

SN - 1003-5214

VL - 18

SP - 225

EP - 227

JO - Jingxi Huagong/Fine Chemicals

JF - Jingxi Huagong/Fine Chemicals

IS - 4

ER -

Synthetises of antioxidant 4,4′-furylidene bisphenol

Abstract

Keywords

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