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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1922Erstellt: 23. Oktober 2026

1,2-Dichloroethane → N-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl Ester

https://huagongshe.com/de/reaction/1922

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktAllyl AlcoholHCID 7858—
EduktEthyl AcetateHCID 8857—
Edukt(R)-3-(benzyloxy)-2-((tert-butoxycarbonyl)amino)propanoic acidHCID 2733693—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(t-Butoxycarbonyl)-O-Benzyl-D-Serine Allyl EsterHCID 53793486—

Reaktionsschritte

N-(t-Butoxycarbonyl)-O-benzyl-D-serine (600 mg; 2.03 mmol) was dissolved in dry methylene chloride (5 ml), allyl alcohol (152 μl; 2.23 mmol) and DMAP (25 mg; 0.20 mmol) added and finally EDC (428.5 mg; 2.24 mmol) added to the acid. The reaction mixture was stirred at room temperature for 2.5 h and the resulting homogeneous solution quenched with water and extracted with methylene chloride. The methylene chloride layer was washed with 5% aqueous citric acid then 10% aqueous sodium carbonate solution. The methylene chloride layer was dried over anhydrous magnesium sulfate powder, filtered and evaporated under reduced pressure to give an oil. Chromatography of the oil using ethyl acetate and hexanes 1:2 v/v afforded the product (408 mg; 60%) as a pale yellow gum. FAB-MS:- Calculated for C36H33N5 335.1; found 336.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726319
Quelldatensatzuspto-grants-1998_03
ORD IDord-36f08b8e5c0c4222ab2cf761a8e66449
Quellennotizuspto-grants-1998_03