La(III)-Catalyzed Depolymerization of Poly(L-Lactic Acid) Yielding Chiral Lactates

Author:

Kobayashi Natsumi1,Komine Nobuyuki1,Nomura Kotohiro2,Hirano Hiroshi3,Hirano Masafumi1

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Nakacho, Koganei, Tokyo 184-8588 , Japan

2. Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, 1-1 Minami-Osawa, Hachioji, Tokyo 192-0397 , Japan

3. Morinomiya Centre, Osaka Research Institute of Industrial Science and Technology, 1-6-50 Morinomiya, Joto-ku, Osaka 536-8553 , Japan

Abstract

Abstract Biomass-based polymers can be a valuable resource of chiral compounds through depolymerization. [La(acac)3]-catalyzed (1 mol%) depolymerization of poly(L-lactic acid) (PLLA) (Mw = 1.58 × 105) pellets in MeOH at 90 °C for 3 h produced methyl L-lactate in >99% yield (96% ee). When powdered PLLA is used, this reaction can be achieved at 40 °C for 6 h in >99% (95% ee). PLLA is depolymerized in EtOH by La(NO3)3·6H2O or [Fe(acac)3] (1 mol%) at 135 °C for 4 h to give ethyl L-lactate in 86% (96% ee) and 87% yield (96% ee), respectively. The depolymerization by [La(acac)3] (5 mol%) in HNEt2 at 150 °C for 3 h gives N,N-diethyllactamide in 85% but the enantiomeric excess decreases to 27% ee.

Publisher

Oxford University Press (OUP)

Subject

General Chemistry

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