HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167913Generated: October 28, 2026
Hydrogen Peroxide → (S)-2-((R)-2-methyl-pentyl)-succinic acid 4-tert-butyl ester
https://huagongshe.com/reaction/1167913
Participants
| Role | Name | HCID | Charge |
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| 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-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidine-3-carbonyl)-octanoic acid tert-butyl ester | HCID 57207445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (S)-2-((R)-2-methyl-pentyl)-succinic acid 4-tert-butyl ester | HCID 21031299 | 93% |
Reaction Steps
To ester 101 (10.8 g, 0.025 mol) in H2O (73 mL) and THF (244 ML) at 0° C. was added a premixed solution of LiOH (51.2 mL of a 0.8 M solution) and H2O2 (14.6 mL of a 30% solution). After 4 hours a further 12.8 mL LiOH (0.8 M solution) and 3.65 mL of H2O2 (30% solution) was added. After 30 minutes sodium bisulfite (7 g), sodium sulfite (13 g), and water (60 mL) was added followed by hexane (100 mL) and ether (100 mL). 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 (300 mL). The resultant solid was filtered off and the filtrate dried (MgSO4) and concentrated to afford an oil (6 g, 93%) which was used without further purification. MS, m/z (relative intensity): 257 [M+H, 100%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620829B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-c7ad8d102aa54586aaa2df0554c4a551 |
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| Source note | uspto-grants-2003_09 |
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