Table 2.
entry | solvent |
cMYR,0 [mol L−1]a |
R [–]b | T [°C] | reaction time [h] | conversion [%]c |
k × 103 [L mol−1 s−1]d |
2.1 | EtOAc | 2.8 | 0.9 | 120 | 2 | 92 | 0.53 |
2.2 | EtOAc | 2.8 | 0.9 | 140 | 2 | 99 | 3.44 |
2.3 | toluene | 2.8 | 0.9 | 100 | 2 | 84 | 0.27 |
2.4 | toluene | 2.8 | 0.9 | 120 | 2 | 95 | 1.14 |
2.5 | toluene | 2.8 | 0.9 | 140 | 2 | 99 | 4.75 |
2.6 | toluene | 2.9 | 1.1 | 160 | 1 | ~100 | 27.05 |
2.7 | toluene | 2.9 | 1.2 | 160 | 1 | ~100 | – |
aInitial myrcene concentration; bratio of myrcene to acrylic acid; cconversions were calculated based on NMR; dk was derived from kinetic studies plotted in Figure 1 for entries 2.1 to 2.6, as in these experiments R was close to 1 (between 0.9 and 1.1).