HuagongsheHuagongshe Chemistry Print Report · For research reference only
Naphthalene → 1,3,6-Naphthalenetrisulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Fuming sulfuric acid | HCID 24681 | — |
| Reactant | Naphthalene-1,3,5-trisulfonic acid | HCID 81165 | — |
| Product | 1,3,6-Naphthalenetrisulfonic acid | HCID 4438 | 21% |
| Product | 1,3,7-Naphthalenetrisulfonic acid | HCID 11970792 | 4% |
Reaction Steps
Naphthalene is introduced at 30° to 35° C. into monohydrate (=100% strength H2SO4), 65% strength oleum being run in at the same time. The reaction mixture is kept at 50° C. for one hour, at 70° C. for one hour and at 90° C. for seven hours, until everything has dissolved. With this process the yield of naphthalene-1,3,5-trisulphonic acid is about 68%, based on the naphthalene employed. In addition, about 21% of naphthalene-1,3,6-trisulphonic acid and about 4 to 5% of naphthalene-1,3,7-trisulphonic acid are formed (see Example 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04369143 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-59df7b0652ed4e688dafa666415fde6a |
| Source note | uspto-grants-1983_01 |