HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(1,1-Dimethylethyl)-1,3-propanediamine → N-(3'-tert-Butylaminopropyl)-aspartic acid-4-ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(1,1-Dimethylethyl)-1,3-propanediamine | HCID 40274 | — |
| Reactant | Monoethyl maleate | HCID 5354457 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(3'-tert-Butylaminopropyl)-aspartic acid-4-ethyl ester | HCID 22817119 | 77.2% |
Reaction Steps
In a manner analogous to that of Example 1, 400 ml of triethylamine are added to 317 g (2.2 mols) of maleic acidmonoethyl ester, and the mixture is subsequently reacted with 260 g (2.0 mols) of 3-tert-butylaminopropylamine. The reaction mixture is further processed as in Example 1 to yield 423.4 g (77.2% of theory) of a white crystalline aspartic acid derivative, which melts at 174°-175° C. after recrystallisation in a mixture of ethanol/acetone (1:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284755 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-bab73897971d413aa15e6d28c1b00fdb |
| Source note | uspto-grants-1981_08 |