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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12593Erstellt: 23. Oktober 2026

Bromide ion → (S)-2-(4-bromobenzyl)amino-3-methylbutyric acid

https://huagongshe.com/de/reaction/12593

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromide ionHCID 259—
EduktL-ValineHCID 6287—
EduktSodium HydroxideHCID 14798—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
Produkt(S)-2-(4-bromobenzyl)amino-3-methylbutyric acidHCID 11673643153,4%

Reaktionsbedingungen

Temperatur22.5 °C

Reaktionsschritte

52 mL (0.21 mol) of N,O-bistrimethylsilylacetamide is added under nitrogen atmosphere to a mixture made up of 23.5 g (0.20 mol) of L-valine and 38.5 mL (0.22 mol) of diisopropylethylamine in 12.5 mL of DMF. After 1 h at 80° C. the suspension changes to a clear solution. Then, in portions and controlling exothermy, 50 g (0.20 mol) of 4-bromobenzylo bromide is added and left to react at 80° C. for 2 h. The mixture is cooled to 20-25° C., 250 mL of toluene and a solution made up of 250 mL of water and 80 mL of NaOH 40% are added. The resulting aqueous phase is washed twice with 100 mL of AcOEt, the remains of solvent distilled and taken to pH 6-7 with HCl 3N. The solid obtained is filtered with 250 mL of IPA to give 43.9 g (76.5%) of N-(4-bromobenzyl)-L-valine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728021B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-145a239c04c24a43b4d3485f843fcd6d
Quellennotizuspto-grants-2010_06