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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430853Erstellt: 24. Oktober 2026

2-((Dimethylamino)methyl)-1-(3-methoxyphenyl)cyclohexanol → Tramadol

https://huagongshe.com/de/reaction/430853

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-((Dimethylamino)methyl)-1-(3-methoxyphenyl)cyclohexanolHCID 5523—
Edukt(2R,3R)-2,3-dihydroxy-2,3-bis(4-methylbenzoyl)butanedioic acidHCID 22860073—
LösungsmittelEthanolHCID 702—
ProduktTramadolHCID 3374197,8%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

The white solid was collected by filtration to give 58.3 g (75.4%) of (L)-(−)-DTTA which compared to an authentic sample. 77.3 g of Di-p-toluoyl-D-tartaric acid ((D)-(+)-DTTA) was taken up in 550 ml of ethanol at 70° C. in a jacketed vessel. To this solution was added the Tramadol free base in 200 ml of ethanol. A precipitate formed almost immediately. The vessel was gradually cooled to 25° C. over several hours to give a fine white solid. Stirring at 25° C. was maintained overnight. The resulting copious white solid was collected at the pump, washing with 500 ml of ethanol. This gave 111.6 g of (+)-Tramadol. Di-p-toluoyl-D-tartaric acid in 85.2% yield, with a de of 97.3%. Reslurrying of this salt from 500 ml of ethanol as above gave 108.5 g of the (+)-Tramadol-containing salt, with a de of >99% in 97.8% yield. [α]D 589=+103.30° (C=1.15, MeOH). MP=162.1-167.8° C. (DSC).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06323368B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-bfb169778fad4603a0f1ef7648eeb019
Quellennotizuspto-grants-2001_11