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HRID 1640519Erstellt: 26. Oktober 2026

Sodium Carbonate → (S)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-oxo-oxazolidine-5-carboxylic acid

https://huagongshe.com/reaction/1640519

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktTempoHCID 2724126—
EduktBis(acetoxy)iodobenzeneHCID 21865429—
Edukt(S)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-5-hydroxymethyl-oxazolidin-2-oneHCID 66736976—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelAcetonitrile--water (1/1)HCID 18373917—
Produkt(S)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-oxo-oxazolidine-5-carboxylic acidHCID 6673628581,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of (S)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-5-hydroxymethyl-oxazolidin-2-one (985 mg, 3.92 mmol) in 1:1 water/MeCN (20 mL) cooled to 0° C. was added diacetoxyiodobenzene (2.83 g, 2.2 eq.) and TEMPO (122 mg, 0.2 eq). The mixture was stirred at 0° C. for 30 min and at rt overnight. EA and sat. Na2CO3 were added and the phases were separated. The aq. layer was washed once more with EA and then carefully acidified with 1M HCl. The water phase was then extracted twice with EA. The combined org. layers were washed with brine and dried over MgSO4 and concentrated to afford the title intermediate as a colourless solid (847 mg, 81% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08114867B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-77ba1dbf9cad4bb3902789dce93097a6
Quellennotizuspto-grants-2012_02