HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 6-Aminonaphthalene-1,3,5-trisulphonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-Amino-5-hydroxynaphthalene-1,7-disulphonic acid | HCID 81024 | — |
| Reactant | 4,5,6-Trifluoro-1,2,3-triazine | HCID 13899144 | — |
| Product | 6-Aminonaphthalene-1,3,5-trisulphonic acid | HCID 6453197 | 200% |
Reaction Steps
31.9 g of 2-amino-5-hydroxynaphthalene-1,7-disulphonic acid are condensed by the procedure of Example 1 with trifluorotriazine and then with morpholine. A diazo compound obtained in the usual manner by direct diazotisation of 38.3 g of 2-aminonaphthalene-1,5,7-trisulphonic acid is added to the resulting suspension of the monofluorotriazinyl compound at 5° to 10°, while simultaneously maintaining the pH at 7.0 to 7.5 by sprinkling in sodium bicarbonate. After coupling is complete, the dyestuff of the formula ##STR17## is salted out, filtered off with suction, dried and milled.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05459245 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-130abafe0e2e4a3c96cefd5c49c5de34 |
| Source note | uspto-grants-1995_10 |