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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129426Erstellt: 27. Oktober 2026

L-Tartaric acid → D-Tartaric acid

https://huagongshe.com/reaction/129426

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-Tartaric acidHCID 444305—
Edukt(4aS-cis-)-6-benzyl-octahydropyrrolo(3.4-b)pyridineHCID 10198297—
Edukt[S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]-nonane L-tartrateHCID 10981401—
Edukt[R,R]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane L-tartrateHCID 68615090—
LösungsmittelDimethylformamideHCID 6228—
ProduktD-Tartaric acidHCID 439655—
Produkt[S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane D-tartrateHCID 22857294—

Reaktionsbedingungen

Temperatur18 °C

Reaktionsschritte

73.6 g (0.34 mol) of cis-8-benzyl-2,8-diazabicyclo[4.3.0]nonane dissolved in 111 ml of dimethylformamide is added a drop at a time to a solution of 102.9 g (0.685 mol) of L(+)-tartaric acid in 343 ml of dimethylformamide. The batch is seeded with [R,R]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane L-tartrate and gradually cooled to an interior temperature of 18° C. The crystals are suctioned off and the filtrate seeded with [S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]-nonane L-tartrate and agitated until it crystallizes completely. ([S,S]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane D-tartrate can be obtained from the mother liquor subsequent to concentration and release of the base by purification with D(-)-tartaric acid as described for Method I.) The product is suctioned off, washed with dimethylformamide and isopropyl alcohol, and dried in the air. The crystals are recrystallized from 88% ethanol. 52 g of [S,S]-8-benzyl-2,8-diazabicyclo[4.3-O]nonane L-tartrate trihydrate are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05468742
Quelldatensatzuspto-grants-1995_11
ORD IDord-a8f57c9f8141442fa246a3b1ec4c906e
Quellennotizuspto-grants-1995_11