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Synthesis of cyclic α-pinane carbonate – a potential monomer for bio-based polymers
Authors:Valentine C. Eze  Abdul Rehman  Manthan Patel  Sajjad Ahmad  Adam P. Harvey
Affiliation:School of Engineering, Newcastle University, Newcastle upon Tyne NE1 7RU UK ; Department of Chemical and Polymer Engineering, University of Engineering and Technology Lahore, Faisalabad Campus, Pakistan,
Abstract:This work reports the first known synthesis of α-pinane carbonate from an α-pinene derivative. Pinane carbonate is potentially useful as a monomer for poly(pinane carbonate), which would be a sustainable bio-based polymer. α-Pinene is a major waste product from the pulp and paper industries and the most naturally abundant monoterpene in turpentine oil. α-Pinene is routinely converted to pinene oxide and pinanediol, but no study has yet demonstrated the conversion of pinanediol into α-pinane carbonate. Here, α-pinane carbonate was synthesised via carboxylation of α-pinanediol with dimethyl carbonate under base catalysis using triazabicyclodecene guanidine (TBD). 81.1 ± 2.8% α-pinane carbonate yield was achieved at 98.7% purity. The produced α-pinane carbonate was a white crystalline solid with a melting point of 86 °C. It was characterised using FTIR, NMR, GCMS and a quadrupole time-of-flight (QTOF) mass spectrometer. The FTIR exhibited a C Created by potrace 1.16, written by Peter Selinger 2001-2019 O peak at 1794 cm−1 confirming the presence of a cyclic carbonate. GCMS showed that the α-pinane carbonate fragments with loss of CO2, forming pinene epoxide. Base hydrolysis of the α-pinane carbonate using NaOH/ethanol/water regenerated the pinanediol with formations of Na2CO3.

Synthesis of α-pinane carbonate from an α-pinene derivative.
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