Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112399Erstellt: 27. Oktober 2026

N,N'-Bis(1-methylethyl)urea → 1-(N-methyl,N-isopropylamino)-3,5-dimethyl-adamantane hydrochloride

https://huagongshe.com/reaction/1112399

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N'-Bis(1-methylethyl)ureaHCID 20084—
Edukt1-Bromo-3,5-dimethyl-adamantane hydrochlorideHCID 22763952—
LösungsmittelWaterHCID 962—
Produkt1-(N-methyl,N-isopropylamino)-3,5-dimethyl-adamantane hydrochlorideHCID 2276395044%

Reaktionsschritte

2.43 grams of 1-bromo-3,5-dimethyl-adamantane hydrochloride were heated in a closed vessel for 40 minutes at 180° C., with 2.8 grams of N,N'-di-isopropylurea. After cooling, the reaction product was suspended in 50 ml. of water, acidified, and extracted with two 10-ml. portions of ether. Next, the water phase was brought to a pH of between 12 and 13 with sodium hydroxide, stirred for 10 minutes, and extracted with four 10-ml. portions of benzene. The benzene extracts were combined, the benzene stripped off, and the residue refluxed for 10 hours with 4 ml. of a 32% formaldehyde solution and 4 ml. of concentrated formic acid. After cooling, the solution was worked up as in Example 6. It yielded 1.04 grams of 1-(N-methyl,N-isopropylamino)-3,5-dimethyl-adamantane hydrochloride. Yield: 38% of theoretical yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04122193
Quelldatensatzuspto-grants-1978_10
ORD IDord-26cf6679e4704e929b7a692564565253
Quellennotizuspto-grants-1978_10