Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 1-Nitroanthraquinone | HCID 6704 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Solvent Red 169 | HCID 33790 | 96.3% |
Reaction Steps
384 g of isopropylamine and 1,390 g of o-xylene are initially introduced into a stainless steel autoclave, which has a capacity of 5 l and is fitted with a stirrer and steam jacket heating, and are heated to 165° C. A suspension of 543 g of 1-nitroanthraquinone with a purity of 98.4% by weight in 815 g of o-xylene is injected into the autoclave in the course of 20 minutes (molar ratio 3:1). During the addition the pressure rises from 10 to 40 bars and the temperature rises from 165 to 170° C. The reaction has ended after a further 30 minutes at 170° C. After cooling and letting-down, the residual solution is evaporated. 548 g of 1-isopropylaminoanthraquinone with a purity of more than 98% are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04163747 |
|---|
| Source dataset | uspto-grants-1979_08 |
|---|
| ORD ID | ord-b3cd1dd05d6d401ba1cc943b3a743f39 |
|---|
| Source note | uspto-grants-1979_08 |
|---|