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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 975280Erstellt: 23. Oktober 2026

Ethyl Acetate → HCID 53715740, Verbindung

https://huagongshe.com/de/reaction/975280

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Eduktp-(Dimethoxymethyl)anisoleHCID 75140—
EduktBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
EduktHCID 53968179HCID 53968179—
LösungsmittelTolueneHCID 1140—
ProduktHCID 53715740HCID 5371574053%

Reaktionsschritte

A solution of 2.07 g of ethyl (2R,3S)-3-cyclopropyl-3-tert-butoxycarbonylamino-2-hydroxypropionate and 213 mg of pyridinium p-toluenesulfonate in 125 ml of toluene is refluxed under heating. To the mixture is added dropwise a solution of 2.76 g of p-anisaldehydedimethylacetal in 25 ml of toluene for 20 minutes. The reaction mixture is evaporated to remove the generated methanol. The mixture is stirred under heating for 1.5 hours and cooled. After the reaction mixture is condensed under reduced pressure, ethyl acetate and water are added to the residue. The ethyl acetate layer is obtained by separation. The aqueous layer is extracted with ethyl acetate. The extract is washed with water and brine, dried and condensed under reduced pressure. The residue is purified by silica gel column chromatography (solvent; toluene:ethyl acetate=40:l) to give 1.572 g of ethyl (4S,5R)-3-tert-butoxycarbonyl-2-(4-methoxyphenyl)-4-cyclopropyl-5-oxazolidinecarboxylate (diastereomeric mixture).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05608073
Quelldatensatzuspto-grants-1997_03
ORD IDord-f643508989c443908e422d065d05ccb4
Quellennotizuspto-grants-1997_03