HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58994Generated: October 29, 2026
Sodium Hydroxide → HCID 117718459, compound
https://huagongshe.com/reaction/58994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(2-Ethylbutoxyl)isophthalaldehyde | HCID 117704583 | — |
| Reactant | HCID 117844841 | HCID 117844841 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 117718459 | HCID 117718459 | — |
Reaction Steps
5-(2-Ethylbutoxyl)isophthalaldehyde (0.20 g, 0.88 mmol) and MeOH (15 mL) were added to a round-bottom flask. To the solution was added N1-(3-aminopropyl)-N3-isobutylpropane-1,3-diamine (0.33 g, 1.76 mmol) and the reaction mixture was stirred for 24 h. Sodium borohydride (0.13 g, 3.52 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 and the reaction mixture stirred for 1 h. The layers were 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 a clear oil.
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-661e34d7ed8243af96827e5e01f17a53 |
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| Source note | uspto-grants-2016_09 |
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