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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349793Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/349793

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
PatentnummerUS07179934B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-9588e0009edb46169dab5a77c0f54ace
Quellennotizuspto-grants-2007_02