HuagongsheHuagongshe Chemistry Print Report · For research reference only
H acid → 2-Aminobenzenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | H acid | HCID 7009 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | HCID 22183044 | HCID 22183044 | — |
| Product | 2-Aminobenzenesulfonic acid | HCID 6926 | — |
Reaction Steps
It is therefore possible, for example, to first acylate a diaminobenzenesulphonic acid with cyanuric chloride, to diazotise the resultant intermediate and to couple it in acid solution to the 1-amino-8-hydroxynaphthalene-3,6-disulphonic acid, to condense the resultant monoazo compound in twice the molar amount with a diaminobenzene and to couple two moles of a diazotised aminobenzenesulphonic acid to the disazo compound which has been formed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03966705 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-e8f66d4b360442859962948b3a57cc8a |
| Source note | uspto-grants-1976_06 |