Synthesis of cyclic α-pinane carbonate - a potential monomer for bio-based polymers

被引:11
|
作者
Eze, Valentine C. [1 ]
Rehman, Abdul [1 ,2 ]
Patel, Manthan [1 ]
Ahmad, Sajjad [2 ]
Harvey, Adam P. [1 ]
机构
[1] Newcastle Univ, Sch Engn, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Univ Engn & Technol Lahore, Dept Chem & Polymer Engn, Faisalabad Campus, Faisalabad, Pakistan
基金
英国工程与自然科学研究理事会;
关键词
RING-OPENING POLYMERIZATION; LIMONENE OXIDE; ETHYL-ESTERS; SAPONIFICATION; CO2; KINETICS; PINENE; DICARBONATE; POLYCARBONATES; ESTERIFICATION;
D O I
10.1039/d1ra07943c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work reports the first known synthesis of alpha-pinane carbonate from an alpha-pinene derivative. Pinane carbonate is potentially useful as a monomer for poly(pinane carbonate), which would be a sustainable bio-based polymer. alpha-Pinene is a major waste product from the pulp and paper industries and the most naturally abundant monoterpene in turpentine oil. alpha-Pinene is routinely converted to pinene oxide and pinanediol, but no study has yet demonstrated the conversion of pinanediol into alpha-pinane carbonate. Here, alpha-pinane carbonate was synthesised via carboxylation of alpha-pinanediol with dimethyl carbonate under base catalysis using triazabicyclodecene guanidine (TBD). 81.1 +/- 2.8% alpha-pinane carbonate yield was achieved at 98.7% purity. The produced alpha-pinane carbonate was a white crystalline solid with a melting point of 86 degrees C. It was characterised using FTIR, NMR, GCMS and a quadrupole time-of-flight (QTOF) mass spectrometer. The FTIR exhibited a C=O peak at 1794 cm(-1) confirming the presence of a cyclic carbonate. GCMS showed that the alpha-pinane carbonate fragments with loss of CO2, forming pinene epoxide. Base hydrolysis of the alpha-pinane carbonate using NaOH/ethanol/water regenerated the pinanediol with formations of Na2CO3.
引用
收藏
页码:17454 / 17465
页数:12
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