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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 651836Erstellt: 27. Oktober 2026

Acetyl chloride → Z-Hse(Ac)-OH

https://huagongshe.com/reaction/651836

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyl chlorideHCID 6367—
EduktCbz-L-HomoserineHCID 489187—
EduktSodium AcetateHCID 517045—
LösungsmittelAcetic AcidHCID 176—
ProduktZ-Hse(Ac)-OHHCID 1183332367,1%

Reaktionsschritte

1.27 g (5 mmol) of N-benzyloxycarbonyl-L-homoserine are dissolved in 5 ml of acetic acid, and 0.41 g (5 mmol) of sodium acetate is added. 1.19 g (15 mmol) of acetyl chloride are then added and stirring is carried out for one hour. The acetic acid and the excess acetyl chloride are removed in vacuo, the residue is taken up in 30 ml of methyl isobutyl ketone and 30 ml of water, and the pH is adjusted to 8 using 50% sodium hydroxide solution. The aqueous phase is separated off, adjusted to pH=2 using hydrochloric acid and extracted using 30 ml of methyl isobutyl ketone. Concentration of the organic phase in vacuo yields 0.99 g (67%) of N-benzyloxycarbonyl—O—acetyl-L-homoserine in the form of a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06281364B1
Quelldatensatzuspto-grants-2001_08
ORD IDord-436e184255444bcf8e6098e637b9f9bb
Quellennotizuspto-grants-2001_08