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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132613Generated: October 24, 2026

Pentanoic Acid → (4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-one

https://huagongshe.com/en/reaction/132613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentanoic AcidHCID 7991—
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantLithium ChlorideHCID 433294—
Reactant4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
SolventTetrahydrofuranHCID 8028—
Product(4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-oneHCID 69269495—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. stirred solution of valeric acid (3.83 mL, 35.2 mmol) and Et3N (14.7 mL, 106 mmol) in dry THF (175 mL) was added trimethylacetyl chloride (5.29 mL, 42.3 mmol) dropwise. The mixture was stirred at 0° C. for 1 hour and (4S,5R)-(−)-4-methyl-5-phenyl-2-oxazolidinone (7.50 g, 42.3 mmol) was added followed by LiCl (1.79 g, 42.3 mmol). The reaction was warmed to room temperature overnight with good stirring. The mixture was filtered and the filtrate was concentrated under reduced pressure. Et2O (75 mL) was added to the residue, which was washed with sat. NaHCO3 (3×40 mL), 1N HCl (3×40 mL), and brine (2×40 mL). The organic phase was dried over MgSO4, filtered and concentrated under reduced pressure to give a quantitative yield of crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388023B2
Source datasetuspto-grants-2008_06
ORD IDord-17bf84a0f9ce45c9bc7ffc3dad778df2
Source noteuspto-grants-2008_06