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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70106Erstellt: 24. Oktober 2026

Methyl iodide → (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid

https://huagongshe.com/de/reaction/70106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktN-[tert-butoxycarbonyl]-L-serineHCID 98766—
EduktSodium ethoxideHCID 2723922—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acidHCID 7016354—

Reaktionsschritte

Under nitrogen a mixture of 74 ml abs. THF and 6 ml abs. methanol is cooled to −70° C. and 2 g sodium hydride (55-65% dispersion) are added. The suspension is stirred for 0.4 hour at ambient temperature. Under nitrogen, 2.05 g N-Boc-L-serine are suspended in 100 ml abs. THF and 40 ml of the prepared sodium ethoxide solution are added. The suspension is stirred for 1 hour at ambient temperature and 1 ml methyliodide are added. After 1 hour the remainder of the sodium ethoxide solution and another 2 ml of methyliodide are added. After 18 hours the reaction mixture is evaporated to dryness. The residue is washed with water and ether and extracted. The water phase is acidified and extracted with ethyl acetate and dichloromethane. 0.52 g of the product are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822474B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-1a7854345f3e4da0922298bdc2c9bd38
Quellennotizuspto-grants-2014_09