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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1636745Erstellt: 25. Oktober 2026

Bromomethylcyclopropane → (4-Bromo-phenyl)-[4-[6-(cyclopropylmethyl-methyl-amino)-hexyloxy]-phenyl]-methanone

https://huagongshe.com/reaction/1636745

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromomethylcyclopropaneHCID 81503—
EduktDiisopropylethylamineHCID 81531—
EduktHCID 10905217HCID 10905217—
LösungsmittelDimethylacetamideHCID 31374—
Produkt(4-Bromo-phenyl)-[4-[6-(cyclopropylmethyl-methyl-amino)-hexyloxy]-phenyl]-methanoneHCID 11059310—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of 0.1 g of (4-bromo-phenyl)-[4-(6-methylamino-hexyloxy)-phenyl]-methanone, 0.13 ml of diisopropylethylamine and 0.06 ml of bromomethyl-cyclopropane in 20 ml of dimethyl-acetamide is stirred at 50° C. for 24 hrs., concentrated and the residue is treated with sodium hydrogen carbonate solution and extracted with methylene chloride. The organic phases are washed with saturated sodium chloride solution, dried and evaporated. The residue is purified over silica gel with CH2Cl2 /MeOH/NH4OH (94/5.410.6 to 85/12.5/2.5). There is obtained 0.68 g of (4-bromo-phenyl)-[4-[6-(cyclopropylmethyl-methyl-amino)-hexyloxy]-phenyl]-methanone which is converted into the fumarate, MS: m/e 443 (M+H+, 1Br).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06034275
Quelldatensatzuspto-grants-2000_03
ORD IDord-ea5080be4d344d63b70fc93e14fff1b6
Quellennotizuspto-grants-2000_03