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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12592Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/12592

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromide ionHCID 259—
EduktL-ValineHCID 6287—
EduktHexamethyldisilazaneHCID 13838—
EduktDiisopropylethylamineHCID 81531—
Eduktp-ToluenesulfonateHCID 85570—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-2-(4-bromobenzyl)amino-3-methylbutyric acidHCID 1167364389%

Reaktionsbedingungen

Temperatur22.5 °C

Reaktionsschritte

To a suspension of 10 g (34.6 mmol) of p-toluenesulphonate of L-valine in 100 mL of CH2Cl2 is added at 20-25° C. and under nitrogen atmosphere 8.0 mL (38 mmol) of 1,1,1,3,3,3-hexamethyldisilazane. After shaking the mixture at 20-25° C. for one hour, 13.2 mL (76 mmol) of diisopropylethylamine and 8.64 g (34.6 mmol) of 4-bromobenzylo bromide are added and heated at reflux. When all the 4-bromobenzylo bromide has been consumed, the solvent is evaporated off at low pressure, 100 mL of water is added and after 1 h at 0° C. the solid is filtered and dried in an air oven at 40° C. to provide 8.8 g (89%) of N-(4-bromobenzyl)-L-valine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728021B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-5759d37bf2144098891bfd299ba656fc
Quellennotizuspto-grants-2010_06