HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethylhexylamine → HCID 178443602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethylhexylamine | HCID 7719 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Product | HCID 178443602 | HCID 178443602 | — |
Reaction Steps
Similarly to the process reported in example 1, the cyanuryl chloride was reacted with 2-ethyl-1-hexylamine, to obtain the corresponding intermediate 2,4-bischloro-6-(2-ethylhexyl)imino-1,3,5-triazine. Similarly to the process reported in examples 2 and 3, the latter was reacted with two equivalents of p-aminobenzoic acid to give the corresponding diacid, which was then converted to the corresponding diacyl chloride by the action of thionyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895731B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-303eacb95df640eab0cb79342a9560db |
| Source note | uspto-grants-2014_11 |