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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950895Generated: October 26, 2026

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

https://huagongshe.com/reaction/1950895

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant(1S,2R)-Cyclohexane-1,2-diamine, N1-BOC protectedHCID 1514389—
SolventAcetonitrileHCID 6342—
Productcis-(2-Pyrrolidin-1-yl-cyclohexyl)-carbamic acid tert-butyl esterHCID 6668088888.1%

Reaction Steps

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)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404673B2
Source datasetuspto-grants-2013_03
ORD IDord-5e0e1221301f4894b1529479b925d73b
Source noteuspto-grants-2013_03