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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132613Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentanoic AcidHCID 7991—
EduktTriethylamineHCID 8471—
EduktPivaloyl chlorideHCID 62493—
EduktLithium ChlorideHCID 433294—
Edukt4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-oneHCID 69269495—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07388023B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-17bf84a0f9ce45c9bc7ffc3dad778df2
Quellennotizuspto-grants-2008_06