Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59003Generated: October 26, 2026

Sodium Hydroxide → N1,N1'-((5-(3-(iso-Butylamino)propoxy)-1,3-phenylene)bis(methylene))-bis(N3-(3-aminopropyl)propane-1,3-diamine)

https://huagongshe.com/reaction/59003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,1-Dimethylethyl N-(3-((3-aminopropyl)amino)propyl)carbamateHCID 2786632—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl (3-(3,5-diformylphenoxy)propyl)(isobutyl)carbamateHCID 131737054—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductN1,N1'-((5-(3-(iso-Butylamino)propoxy)-1,3-phenylene)bis(methylene))-bis(N3-(3-aminopropyl)propane-1,3-diamine)HCID 117718429—

Reaction Steps

tert-Butyl (3-(3,5-diformylphenoxy)propyl)-(isobutyl)carbamate (0.15 g, 0.42 mmol) and MeOH (10 mL) were added to a round-bottom flask. To the solution was added tert-butyl (3-((3-aminopropyl)amino)propyl)carbamate (0.20 g, 0.84 mmol) and the reaction mixture was stirred for 24 h. Sodium borohydride (0.06 g, 1.69 mmol) was added and the reaction mixture stirred for 1 h. The reaction mixture was concentrated under reduced pressure to afford a white solid. Aqueous NaOH (10%, 50 mL) and EtOAc (50 mL) were added, the layers separated and the aqueous layer was extracted with EtOAc (50 mL). The organic layers were combined, dried over Na2SO4, filtered, and concentrated under reduced pressure to afford the desired product as clear oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439433B2
Source datasetuspto-grants-2016_09
ORD IDord-9b0cd479e0d445cfba4b323909771052
Source noteuspto-grants-2016_09