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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76844Erstellt: 23. Oktober 2026

2-Amino-3,3-dimethylbutanoic acid → D-tert-leucine

https://huagongshe.com/de/reaction/76844

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Amino-3,3-dimethylbutanoic acidHCID 306131—
EduktDibezoyl-D-tartaric acid monohydrateHCID 122598382—
LösungsmittelWaterHCID 962—
ProduktD-tert-leucineHCID 695034092%

Reaktionsbedingungen

Temperatur28 °C

Reaktionsschritte

(DL)-tert-Leucine (15 g, 0.1145 mol) was dissolved in water (180 mL). To the solution was added dibenzoyl-d-tartaric acid monohydrate (21.5 g, 0.057 mol) and stirred for 24 hours at 28° C. (±3). The reaction mixture was filtered to collect L-tert-leucine dibenzoyl-d-tartrate salt. The filtrate was reserved for isolating D-tert-leucine later. The tartrate salt was added to water (150 mL) followed by concentrated sulphuric acid (3 mL) and stirred for 4 hours. Liberated dibenzoyl-d-tartaric acid was collected and dried (19.8 g, 92% yield). The filtrate was washed with diisopropyl ether (50 mL) to remove any traces of dibenzoyl-d-tartaric acid, cooled to 5° C. and treated with a saturated solution of barium hydroxide till the pH was neutral. It was filtered to remove the precipitated barium sulphate. The filtrate was concentrated under reduced pressure to remove all the solvent. The residue obtained was stirred with acetone (15 mL×2), filtered and dried to obtain colorless solid L-tert-leucine (6 g, 80% yield, 99% chemical purity, 99.9% chiral purity).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08835676B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-ddb0d8bc251843a794ab7a67a49c4307
Quellennotizuspto-grants-2014_09