HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 68126044, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | m-Toluidine | HCID 7934 | — |
| Reactant | HCID 21400469 | HCID 21400469 | — |
| Product | HCID 68126044 | HCID 68126044 | — |
Reaction Steps
If the procedure indicated above is followed but the 8-nitro compound is replaced by a mixtue of 1-isopropylamino-4-bromo-5- and -8-nitroanthraquinone and 180 g of p-anisidine are used instead of m-toluidine as the base, 48 g of a mixture consisting of 1-isopropylamino-4-p-anisidino-5-nitroanthraquinone and 1-isopropylamino-4-p-anisidine-8 -nitroanthraquinone are obtained after dilution with 300 ml of methanol and filtration at 10°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04056544 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-f8ff3336ab75439aa82a034ddf385e2e |
| Source note | uspto-grants-1977_11 |