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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 659182Erstellt: 24. Oktober 2026

1,4-Dibromobutane → cis-(2-Pyrrolidin-1-yl-cyclohexyl)-carbamic acid tert-butyl ester

https://huagongshe.com/de/reaction/659182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DibromobutaneHCID 8056—
EduktPotassium CarbonateHCID 11430—
Edukt(1S,2R)-Cyclohexane-1,2-diamine, N1-BOC protectedHCID 1514389—
LösungsmittelAcetonitrileHCID 6342—
Produktcis-(2-Pyrrolidin-1-yl-cyclohexyl)-carbamic acid tert-butyl esterHCID 6668088888,1%

Reaktionsschritte

1-N-Boc-1,2-cis-cyclohexyldiamine 5 (CAS 184954-75-4) (1.65 g, 7.7 mmol) was dissolved in 100 mL acetonitrile. Potassium carbonate (5.3 g, 39 mmol) and 1,4-dibromobutane (2.8 g, 13 mmol) were added and the reaction mixture was refluxed overnight. The solvent was evaporated off. The residue was taken up in water and ethyl acetate and was extracted three times with ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (dichloromethane/methanol/ammonia 100:0:0→140:10:1) yielded cis-(2-pyrrolidin-1-yl-cyclohexyl)-carbamic acid tert-butyl ester as a yellow liquid (1.82 g, 88%), MS: m/e=269.4 [(M+H)+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08080541B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-9cf38beef3ff40eebc6de1ccba63f616
Quellennotizuspto-grants-2011_12