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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 61416Erstellt: 24. Oktober 2026

Sodium Iodide → 1-Benzyl 4-(tert-Butyl) N-Benzyl-N-(2-(chloromethyl)allyl)-L-aspartate

https://huagongshe.com/de/reaction/61416

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktPotassium CarbonateHCID 11430—
Edukt3-Chloro-2-chloromethyl-1-propeneHCID 15859—
Edukt1-Benzyl 4-(tert-butyl) benzyl-L-aspartateHCID 16069553—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Benzyl 4-(tert-Butyl) N-Benzyl-N-(2-(chloromethyl)allyl)-L-aspartateHCID 1606955458,3%

Reaktionsbedingungen

Temperatur81 °C

Reaktionsschritte

A mixture of (2S)-benzylamino-succinic acid 1-benzyl ester 4-tert-butyl ester (12.1 g, 32.6 mmol), K2CO3 (14 g, 3 equiv.), NaI (3.0 g, 20 mmol) and 3-chloro-2-chloromethyl-1-propene (5.1 g, 40.8 mmol) in MeCN (150 mL) was stirred at 81° C. for 16 h. After cooling, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Purification by Combiflash (hexane and ethyl acetate: gradient 0 to 8% during 12 min) afforded (2S)-[benzyl-(2-chloromethyl-allyl)-amino]-succinic acid 1-benzyl ester 4-tert-butyl ester (8.7 g, 58%). MS (ESI): 458 (M+Na+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440958B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-0aa6f41428f748ed803e2853f83968ea
Quellennotizuspto-grants-2016_09