HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → (S)-2-((R)-2-Methyl-butyl)-succinic Acid 4-tert-butyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | (3S,5R)-5-Methyl-3-[1-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-yl)-methanoyl]-heptanoic acid tert-butyl ester | HCID 66939639 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-((R)-2-Methyl-butyl)-succinic Acid 4-tert-butyl Ester | HCID 54311211 | 100% |
Reaction Steps
To ester 112 (7.26 g, 0.018 mol) in H2O (53 mL) and THF (176 mL) at 0° C. was added a premixed solution of LiOH (37 mL of a 0.8 M solution) and H2O2 (10.57 mL of a 30% solution) and the solution warmed to room temperature. After 2 hours sodium bisulfite (7 g), sodium sulfite (13 g), and water (60 mL) was added and the two layers were separated and the aqueous layer extracted with ether. The combined organic phases were concentrated to an oil that was dissolved in heptane (200 mL). The resultant solid was filtered off and the filtrate dried (MgSO4) and concentrated to afford an oil (4.4 g) that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189747B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-dbe614aca2fd4927966468d90872d847 |
| Source note | uspto-grants-2007_03 |