HuagongsheHuagongshe Chemistry Print Report · For research reference only
Keto-pantoyllactone → D-Pantolactone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Keto-pantoyllactone | HCID 39 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | N,N,N-Tributylbutan-1-aminium trifluoroacetate | HCID 3084618 | — |
| Reactant | (2S,4S)-(-)-N-BOC-4-Diphenylphosphino-2-diphenylphosphinomethyl-pyrrolidine | HCID 10209545 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | D-Pantolactone | HCID 439368 | — |
Reaction Steps
A 500 ml steel autoclave was loaded in a glove box (O2 -content less than 1 ppm) with 40.0 g (0.31 mol) of ketopantolactone, 210 ml of toluene, 180.6 mg (0.389 mmol) of [Rh(COD)2 ]PF6, 237.3 mg (0.389 mmol) of mCH3 --BPPM and 138.3 mg (0.389 mmol) of tetrabutylammonium trifluoroacetate. The hydrogenation was carried out at a constant pressure of 40 bar of H2 at 30° C. and with intensive stirring. By virtue of the exothermic reaction the temperature rose to 55° C. A conversion of above 99% was achieved after 1.2 hours. After a total hydrogenation time of 2 hours the mixture was worked-up as described in Example 2. Pure (R)-pantolactone was obtained. [α]D20 =-46.0°. Optical purity 89.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04652657 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-c20e25a16536471ca51a82d1ff149b83 |
| Source note | uspto-grants-1987_03 |