DL-Homoserine → (RS)-2-(4-chlorobenzenesulfonylamino)-4-butanolide

HRID 266354

Reaktionsgleichung

Reaktionsgleichung von HRID 266354
[NH2:1][CH:2]([CH2:6][CH2:7][OH:8])[C:3]([OH:5])=O.C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C.[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:24][CH:23]=1>O.C1COCC1>[Cl:21][C:22]1[CH:27]=[CH:26][C:25]([S:28]([NH:1][CH:2]2[CH2:6][CH2:7][O:8][C:3]2=[O:5])(=[O:30])=[O:29])=[CH:24][CH:23]=1

Komponenten

7

Edukt 4

HCID 779DL-HomoserineHCID 73984-Chlorobenzenesulfonyl chlorideHCID 8857Ethyl AcetateHCID 11430Potassium Carbonate

Produkt 1

HCID 19032731(RS)-2-(4-chlorobenzenesulfonylamino)-4-butanolideAusbeute 60,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

(RS)-2-amino-4-hydroxybutanoic acid (2.0438 g) was dissolved in water (20 ml). The solution was cooled to 0° C., and potassium carbonate (5.217 g) and ethyl acetate (20 ml) were added. Then, p-chlorobenzenesulfonyl chloride (9.0536 g) and THF (2 ml) were added, and the whole was stirred overnight. After the reaction was completed, the ethyl acetate layer was separated. The aqueous layer was acidified with 2N HCl and extracted with ethyl acetate. The combined ethyl acetate layers were concentrated to give a crude product. The crude product was purified by silica gel column chromatography (silica gel 50 g, hexane/ethyl acetate=2/1) to obtain (RS)-2-(4-chlorobenzenesulfonylamino)-4-butanolide (2.8674 g).

Aufarbeitung

  1. customthe ethyl acetate layer was separated
  2. extractionextracted with ethyl acetate
  3. concentrationThe combined ethyl acetate layers were concentrated
  4. customto give a crude product
  5. customThe crude product was purified by silica gel column chromatography (silica gel 50 g, hexane/ethyl acetate=2/1)

Quellen und Nachweise

ORD-Eintrag
ord-b9c6c5a45e164ac8aa66d3c6f2f83ebc
Quelldatensatz
uspto-grants-1997_07
Patentnummer
US05650428

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