HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dimethylaniline → HCID 13763883, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dimethylaniline | HCID 7949 | — |
| Reactant | HCID 20205653 | HCID 20205653 | — |
| Product | HCID 13763883 | HCID 13763883 | 56% |
Reaction Steps
1-anilino-4-(3,5-dimethylanilino)anthraquinone was prepared by reaction of 3,5-dimethylaniline with 1-(anilino)-4-tosylanthraquinone. The isolated and purified reaction product has the structure illustrated below. ##STR16## The yield was 56% and m.p. 219.5°-220.5° C. Mass spectrum, m/e 418 (M+); H-NMR (CD2Cl2)δ12.20 (br s, 2H), 8.41-8.30 (m, 2H) 7.80-7.69 (m, 2H), 7.52-7.34 (m, 7H), 6.90 (br s, 3H), 2.32 (s, 6H); UV/VIS max (Xylenes) 404 nm (ε6 600), 600 (13 400), 641 (14 400).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04661293 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-0bb92c0c5dfb4164a2bb421ae3ba7e7e |
| Source note | uspto-grants-1987_04 |