HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(2-aminoethyl)-8-dimethylamino-6,6-diphenyl-5-hydroxynonylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 2-Dimethylamino-4,4-diphenyl-5-oxononanal | HCID 19981507 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-aminoethyl)-8-dimethylamino-6,6-diphenyl-5-hydroxynonylamine | HCID 19981504 | — |
Reaction Steps
Ethylenediamine was added to a solution of 2-dimethylamino-4,4-diphenyl-5-oxononanal (12 mg), as prepared in Example 1, in methanol (0.5 ml). After the mixture was stirred at room temperature, sodium cyanoborohydride (10 mg) was added. The mixture was stirred at room temperature for 18 hours, water was added, and the aqueous mixture was extracted with chloroform. The combined extracts were washed with brine and dried (MgSO4). Rotary evaporation gave a crude product which was further dried in vacuo to yield 4 mg of N-(2-aminoethyl)-8-dimethylamino-6,6-diphenyl-5-hydroxynonylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05073629 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-2e4f68c48f8b4e7ca52b97dcfd833cdb |
| Source note | uspto-grants-1991_12 |