HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethyl-1,3-propanediamine → N-(3'-Dimethylaminopropyl)-aspartic acid-4-n-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | Monobutyl maleate | HCID 5356726 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(3'-Dimethylaminopropyl)-aspartic acid-4-n-butyl ester | HCID 86738344 | 86.8% |
Reaction Steps
In the apparatus described in Example 1, 500 ml of triethylamine are added with cooling, within 2 hours and 35 minutes, at 4°-10° C. internal temperature to 430.5 g (2.5 mols) of maleic acid-mono-n-butyl ester. There are subsequently quickly added 306.5 g (2.5 mols+20% excess) of 3-dimethylaminopropylamine, and the mixture is reacted for 30 minutes at 90°-95° C. The reaction product is processed in a manner analogous to that described in Example 1 to obtain a yield of 595 g (86.8% of theory) of a crystalline aspartic acid derivative, which melts at 154°-157.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04326069 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-aea21b7460aa42a1971de9aa04474c6b |
| Source note | uspto-grants-1982_04 |