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. 2018 Sep 12;57(41):13449–13453. doi: 10.1002/anie.201808676

Table 2.

Hydrogenation of cyclic carbonates using Mn complex 1 as a pre‐catalyst.[a,b] Inline graphic

Entry Carbonate [Mn]
[mol %]
Conv.
[%]
Diol
[7, %]
Methanol
[8, %]
1 graphic file with name ANIE-57-13449-g006.jpg 6 b 1 89 75 66
2 2 >99 82 75
3 graphic file with name ANIE-57-13449-g007.jpg 6 c 1 86 82 65
4 2 >99 97 74
5 graphic file with name ANIE-57-13449-g008.jpg 6 d 1 82 76 66
6[c] graphic file with name ANIE-57-13449-g009.jpg 6 e 1 67 59 43
7[c] 2 77 71 60
8 graphic file with name ANIE-57-13449-g010.jpg 6 f 1 79 58 41
9 2 97 80 75
10 graphic file with name ANIE-57-13449-g011.jpg 6 g 1 >99 98 94
11 graphic file with name ANIE-57-13449-g012.jpg 6 h 1 80 73 57

[a] Conditions: 6 (0.5 mmol), H2 (30 bar), complex 1, NaOtBu (1.1 equiv with respect to 1), THF (0.7 mL), temp. (120 °C), 26 h. [b] Yield was calculated using gas chromatography, ethyl heptanoate (25 μL, 0.15 mmol) was used as an internal standard. [c] 1,3‐Propanediol (25 μL, 0.34 mmol) was used as an internal standard.