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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,1-Dimethylethyl N-(3-((3-aminopropyl)amino)propyl)carbamate | HCID 2786632 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | tert-Butyl (3-(3,5-diformylphenoxy)propyl)(isobutyl)carbamate | HCID 131737054 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N1,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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09439433B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-9b0cd479e0d445cfba4b323909771052 |
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| Source note | uspto-grants-2016_09 |
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