HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → HCID 20201040, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19418158 | HCID 19418158 | — |
| Product | HCID 20201040 | HCID 20201040 | — |
Reaction Steps
9.5 Parts of 1,4-diketo-3,6-di-(4'-methylphenyl)pyrrolo-[3,4-c]-pyrrole, 9 parts of anhydrous potassium carbonate, 24 parts of methyl p-toluenesulfonate and 110 parts of nitrobenzene are stirred at 200° C. for 1/2 hour. After the mixture has been cooled, the dye is filtered off and washed with a little nitrobenzene and then with methanol and hot water. After drying, 5.8 parts of 1,4-diketo-2,5-dimethyl-3,6-di-(4'-methylphenyl)-pyrrolo-[3,4-c]-pyrrole are obtained in the form of yellowish-tinged red crystals of melting point 260° C. (formula XIV). The dye gives pure yellow shades of good fastness properties on PES by the method described in Example 1. ##STR18##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666455 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-f56a3a675c624464a4df97a47e24a243 |
| Source note | uspto-grants-1987_05 |