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HRID 538921Erstellt: 24. Oktober 2026

4-Methylmorpholine → Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoate

https://huagongshe.com/de/reaction/538921

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktIsobutyl chloroformateHCID 62365—
EduktN-tert-Butoxycarbonyl-L-aspartic acid beta-benzyl esterHCID 1581888—
EduktSodium borohydrideHCID 4311764—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktPhenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoateHCID 10040985—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

To a solution of Boc-L-aspartic acid-4-benzyl ester (100 g, 309 mmol) in DME (1.8 L) at −20° C. was added NMM (34 mL, 309 mmol) then dropwise iso-butylchloroformate (40 mL, 309 mmol) and the mixture was stirred at −20° C. for 20 min. The reaction mixture was filtered and the filtrate was cooled to −20° C. NaBH4 (17.5 g, 463 mmol) was added portionwise at −20° C. The mixture was allowed to warm and stirred at rt for 1 h. The mixture was quenched with a 20% citric acid solution and then extracted with AcOEt. The organic layer was washed with NaHCO3 solution, H2O and brine, dried (MgSO4), filtered and concentrated. The product was used without further purification for the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08865894B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-379a98ce8165465aad03657a829ab132
Quellennotizuspto-grants-2014_10