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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216666Generated: November 1, 2026

Hydrogen Peroxide → (S)-2-((R)-2-methyl-pentyl)-succinic acid 4-tert-butyl ester

https://huagongshe.com/reaction/2216666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantLithium HydroxideHCID 3939—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BisulfiteHCID 23665763—
Reactant(3S,5R)-5-Methyl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidine-3-carbonyl)-octanoic acid tert-butyl esterHCID 57207445—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(S)-2-((R)-2-methyl-pentyl)-succinic acid 4-tert-butyl esterHCID 2103129993%

Reaction Steps

To (3S,5R)-5-methyl-3-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidine-3-carbonyl)-octanoic acid tert-butyl ester (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 (S)-2-((R)-2-methyl-pentyl)-succinic acid 4-tert-butyl ester (6 g, 93%) which was used immediately without further purification. MS, m/z (relative intensity): 257 [M+H, 100%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112610B2
Source datasetuspto-grants-2006_09
ORD IDord-83a5496852034369998eeb42bb4cf5e2
Source noteuspto-grants-2006_09