HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → P-Phenylenediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 12956245 | HCID 12956245 | — |
| Reactant | HCID 20194322 | HCID 20194322 | — |
| Product | P-Phenylenediamine | HCID 7814 | — |
| Product | 1,4-Anthracenedione, 2,3-dihydro-9,10-dihydroxy- | HCID 87211 | — |
Reaction Steps
1 part of 4-chlorosulphonyl phthalic acid is added to a solution of 0.5 parts of 1-hydroxy-4-(4-aminoanilino)-anthraquinone, (itself obtained by the reaction of leucoquinizarin with 4-phenylene diamine) in 25 parts of dioxan. The mixture is heated under reflux for 51/2 hours, filtered hot, and the filtrate poured into water. The precipitated product is filtered off, dissolved in dilute sodium carbonate solution at 20°C, screened, and the filtrate acidified with mineral acid to give 0.4 parts of 1-hydroxy-4-[4-(3,4-dicarboxy phenylsulphonylamino)anilino]anthraquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03934972 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-522bf73489354a3a812cccf8c9222168 |
| Source note | uspto-grants-1976_01 |