HuagongsheHuagongshe Chemistry Print Report · For research reference only
Keto-pantoyllactone → (+-)-Pantolactone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Keto-pantoyllactone | HCID 39 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (+-)-Pantolactone | HCID 989 | — |
Reaction Steps
2-Oxo-3,3-dimethyl-γ-butyrolactone (18) was hydrogenated according to General Procedure B in THF at 20.7 barg (300 psig) hydrogen at ambient temperature using bis(1,5-cyclooctadiene)rhodium trifluoromethanesulfonate (2.3 mg; 5 μmol; 0.01 equiv) and ligand (S,R)-2g (3.7 mg; 6 μmol; 0.012 equiv) for 6 hours to afford 99.6% conversion to 2-hydroxy-3,3-dimethyl-γ-butyrolactone (19) with 97.2% ee as determined by chiral GC analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06590115B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-308df87afbe0408eb592b3fb3c3ae21d |
| Source note | uspto-grants-2003_07 |