HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 1,2-Ethanediamine, N1-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Aziridine | HCID 9033 | — |
| Product | 1,2-Ethanediamine, N1-phenyl- | HCID 74270 | 13% |
Reaction Steps
It is known to produce certain unsymetrically substituted 1,2-ethanediamines. Current processes, however, have proven unacceptable. For example, G. I. Braz et al. disclosed that the aminoethylation of aniline with ethyleneimine afforded only a 13 percent yield of N-phenyl-1,2-ethanediamine. The remaining product comprised polyamino ethyl compounds of high molecular weight. Dokl. Akad. Nauk., 59, 489 (1948), Chem. Abstr., 42, 6747 (1948).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04381401 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-e634b142c5f5483dbfd76b394b492727 |
| Source note | uspto-grants-1983_04 |