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HRID 66560Erstellt: 24. Oktober 2026

Ammonia → (+/-)-2-Benzyl-2-(3'-dimethylaminopropoxy)-1,7,7-trimethyl-bicyclo(2,2,1) heptane

https://huagongshe.com/de/reaction/66560

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktHydrochloric AcidHCID 313—
Edukt2,3-Dihydroxybutanedioic AcidHCID 875—
EduktAmmonium HydroxideHCID 14923—
EduktSodium amideHCID 24533—
Edukt3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
Edukt2-Benzyl-1,7,7-trimethylbicyclo[2.2.1]heptan-2-olHCID 251172—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
Produkt(+/-)-2-Benzyl-2-(3'-dimethylaminopropoxy)-1,7,7-trimethyl-bicyclo(2,2,1) heptaneHCID 13749826—

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

A suspension of 3.9 g (0.1 mole) of sodium amide in 100 ml of anhydrous benzene is heated to boiling, and a solution of 24.4 g (0.1 mole) of (±)-2-benzyl-1,7,7-trimethyl-bicyclo(2,2,1)-heptan-2-ol in 100 ml of anhydrous benzene is added dropwise, under continuous stirring. When the addition of the above solution is completed the reaction mixture is boiled until the formation of ammonia gas is ceased, and while further continuing the stirring, a solution of 13.4 g (0.11 mole) of 1-dimethylamino-3-chloro-propane in 20 ml of anhydrous benzene is added. After boiling the mixture for further 6 hours it is cooled to 30° C., washed three times with 40 ml of water each, and extracted with a solution of 15 g (0.1 mole) of tartaric acid in 50 ml of water or with 0.11 mole of diluted aqueous hydrochloric acid. The aqueous solution cooled to 0°-5° C. is made alkaline to pH 10 with concentrated ammonium hydroxide. The base separated as an oil is extracted with dichloroethane. On distilling off the solvent, the residue is fractionated in vacuo.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04342762
Quelldatensatzuspto-grants-1982_08
ORD IDord-138ae41e29694560a93721ec503396c0
Quellennotizuspto-grants-1982_08