Naturally Occurring α-Amino Acid Catalyzed Coupling of Carbon Dioxide with Epoxides to Afford Cyclic Carbonates

Abstract

A new and simple method was developed by using the naturally occurring α-amino acids as catalyst for the efficient coupling of carbon dioxide with epoxides to afford the corresponding cyclic carbonates. The cooperation of the ammonium group of one amino acid and the carboxylate ion of another one were proposed as a key activation factor for this transformation.

amino acids - epoxides - carbon dioxide - coupling reaction - cyclic carbonates

References and Notes

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5

Typical Experimental Procedure: Propylene oxide (20 mmol), l-phenylalanine (0.16 mmol) and CH₂Cl₂ (1 mL) were added into a 15 mL stainless autoclave with a magnetic stirrer, and CO₂ (liquid, 3.2 MPa) was charged into the reactor at r.t. The initial pressure was generally adjusted to 6 MPa at 130 °C. The autoclave was heated at that temperature for 48 h, and the pressure was kept constant during the reaction. After the reaction, the reactor was cooled to 0 °C, and extra CO₂ was vented slowly. The crude product was analyzed by a gas chromatograph, compared with authentic sample, and the yields were determined by GC using tridecane as internal standard. The crude product (yield: 100% by GC) was purified by distillation and propylene carbonate was obtained in 93% isolated yield. The cyclic carbonate was identified by IR, GC/MS (HP6890/5973) and 400 MHz NMR spectroscopy.

6

Spectroscopic data of the cyclic carbonates:
4-Methyl-1,3-dioxolan-2-one (2a): IR (neat): 1795 (C=O) cm^-1. MS (EI): m/z = 102 [M⁺]. ¹H NMR (400 MHz, TMS, CDCl₃): δ = 1.48 (d, J = 3.6 Hz, 3 H, CH₃), 4.01 (t, J = 8.4 Hz, 1 H, CH), 4.53 (t, J = 8.0 Hz, 1 H, CH), 4.81-4.86 (m, 1 H, CH).
4-Chloromethyl-1,3-dioxolan-2-one (2b): IR (neat): 1790 (C=O) cm^-1. MS (EI): m/z = 136 [M⁺]. ¹H NMR (400 MHz, TMS, CDCl₃): δ = 3.72-3.74 (m, 2 H, CH₂), 4.38 (q, J = 6.0 Hz, 1 H, CH), 4.57 (t, J = 8.4 Hz, 1 H, CH), 4.91-4.94 (m, 1 H, CH).
4-Phenyl-1,3-dioxolan-2-one (2c): IR (neat): 1816 (C=O) cm^-1. MS (EI): m/z = 164 [M⁺]. ¹H NMR (400 MHz, TMS, CDCl₃): δ = 4.31-4.35 (m, 1 H, CH), 4.76-4.82 (m, 1 H, CH), 5.66 (t, J = 8.0 Hz, 1 H, CH), 7.32-7.44 (m, 5 H, C₆H₅).
4-Butyl-1,3-dioxolan-2-one (2d): IR (neat): 1798 (C=O) cm^-1. MS (EI): m/z = 145 [M⁺]. ¹H NMR (400 MHz, TMS, CDCl₃): δ = 0.91 (t, J = 4.8 Hz, 3 H, CH₃), 1.32-1.38 (m, 4 H, CH₂), 1.65-1.78 (m, 2 H, CH₂), 4.04 (dd, J = 7.2, 8.4 Hz, 1 H, CH), 4.50 (t, J = 8.0 Hz, 1 H, CH), 4.64-4.71 (m, 1 H, CH).
4-Phenoxymethyl-1,3-dioxolan-2-one (2e): IR (neat): 1796 (C=O) cm^-1. MS (EI): m/z = 194 [M⁺]. ¹H NMR (400 MHz, TMS, CDCl₃): δ = 4.13 (dd, J = 3.6, 10.4 Hz, 1 H, CH), 4.22 (dd, J = 4.0, 10.4 Hz, 1 H, CH), 4.52 (dd, J = 6.0, 8.8 Hz, 1 H, CH), 4.60 (t, J = 4.4 Hz, 1 H, CH), 4.99-5.02 (m, 1 H, CH), 6.89 (d, J = 7.6 Hz, 2 H, Ph), 7.00 (t, J = 7.6 Hz, 1 H, Ph), 7.29 (dd, J = 7.6, 8.4 Hz, 2 H, Ph).
4-Allyloxymethyl-1,3-dioxolan-2-one (2f): IR (neat): 1796 (C=O) cm^-1. MS (EI): m/z = 159 [M⁺ + H]. ¹H NMR (400 MHz, TMS, CDCl₃): δ = 3.21-3.68 (m, 2 H, CH₂), 4.02-4.04 (m, 2 H, CH₂), 4.37 (dd, J = 6.0, 8.4 Hz, 1 H, CH), 4.48 (t, J = 8.4 Hz, 1 H, CH), 4.75-4.80 (m, 1 H, CH), 5.18-5.28 (m, 2 H, CH₂), 5.81-5.87 (m, 1 H, CH).
Cyclohexyl-1,3-dioxolan-2-one (2g): IR (neat): 1801 (C=O) cm^-1. MS (EI): m/z = 142 [M⁺]. ¹H NMR (400 MHz, TMS, CDCl₃): δ = 1.37-1.41 (m, 2 H, CH₂), 1.57-1.61 (m, 2 H, CH₂), 1.85-1.89 (m, 4 H, CH₂), 4.63-4.68 (m, 2 H, CH).

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