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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604760Generated: October 30, 2026

tert-butyl N-(4-aminobutyl)carbamate → HCID 85975644, compound

https://huagongshe.com/reaction/604760

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium HydroxideHCID 14923—
Reactant4-BromobutyronitrileHCID 21412—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductHCID 85975644HCID 8597564468.1%

Reaction Steps

To a solution of the BOC protected diamine 9 (2.10 g, 0.01 mol) in anhydrous acetonitrile (50 mL) was added potassium carbonate (5.14 g) and the suspension was stirred at RT for 10 minutes. A solution of 4-bromobutyronitrile (1.65 g, 0.01 mol) in acetonitrile (25 mL) was added and the resulting mixture stirred at 50° C. for 24 hours. TLC (1:10:89 NH4OH:MeOH:CHCl3) showed that the reaction was 95% complete. The mixture was filtered to remove most of the inorganic salts and the acetonitrile was removed in vacuo to give a solid/oily residue that was purified by flash column chromatography (1:5:94 NH4OH:MeOH:CHCl3) to yield the product 10 as a clear oil (1.74 g, 61%), Rf=0.5 (1:10:89 NH4OH:MeOH:CHCl3); 1H NMR (CDCl3) d 4.79 (br s, 1H, NHCO), 3.12 (q, 2H, CH2), 2.74 (t, 2H, CH2), 2.60 (t, 2H, CH2), 2.46 (t, 2H, CH2), 1.81 (quin, 2H, CH2) 1.57-1.37 (m, 13H, 2×CH2, 3×CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910363B1
Source datasetuspto-grants-2011_03
ORD IDord-316cb1aee89b402c84d11f5313472cc2
Source noteuspto-grants-2011_03