Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 1,3,6-Naphthalenetrisulfonic acid | HCID 4438 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Naphthalene | HCID 931 | — |
Reaction Steps
For example, the industrially important 8-nitronaphthalene-1,3,6-trisulphonic acid (nitro-T-acid) is prepared by nitrating the isomer mixture of naphthalenetrisulphonic acids which is obtained in the trisulphonation of naphthalene with sulphuric acid and oleum and contains, as the main constituent, naphthalene-1,3,6-trisulphonic acid, with nitric acid in sulphuric acid, as the solvent (see F.I.A.T., Final Report 1016, pages 32-39). In the preparation process known from the literature, a procedure is followed in which the hot solution of the naphthalenetrisulphonic acids in sulphuric acid, which solution has a temperature of 150° to 155° C. and is obtained in the trisulphonation of naphthalene, is cooled to 100° C., diluted with water and cooled further to 80° C. The batch is then transferred to the nitration kettle, cooled in this kettle to 35° to 40° C. and nitrated with mixed acid (86% of nitric acid, 12% of sulphuric acid and 2% of water) at 35° to 40° C. in the course of about 10 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04534905 |
|---|
| Source dataset | uspto-grants-1985_08 |
|---|
| ORD ID | ord-f8a36de0a6514cf7ac85a554494208c3 |
|---|
| Source note | uspto-grants-1985_08 |
|---|