HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859210Generated: October 31, 2026
Hydrochloric Acid → Anthracene, 2-methyl-9-nitro-
https://huagongshe.com/reaction/1859210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 2-Methylanthracene | HCID 11936 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Anthracene, 2-methyl-9-nitro- | HCID 190418 | — |
Reaction Steps
Synthesis of 2-methyl-9-nitroanthracene ##STR12## Nitration of 2-methylanthracene (Source Aldrich) was carried out using the same procedure as in example 1 to yield the 2-methyl-9-nitroanthracene as a yellow solid. 2-Methylanthracene (2.0 g; 0.010 mole) was suspended in glacial acetic acid (25 ml) and to the stirred solution was added concentrated nitric acid (0.6 ml; 0.014 mole). The solution was stirred in a water bath at 20-25° C. for 4 hours, until the solution became clear. To the clear solution a mixture of conc. HCl and acetic acid (20 ml; 1:1) was added via a dropping funnel over a period of 15 minutes. A yellow solid precipitated out. The solution was stirred for further 30 minutes and filtered under suction. The product was treated by the same method as described in example 1 to give the 2-methyl-9-nitroanthracene as a yellow solid (1.8 g; 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06153726 |
|---|
| Source dataset | uspto-grants-2000_11 |
|---|
| ORD ID | ord-4967da2f40f3471c8afe5f2ef247bcf9 |
|---|
| Source note | uspto-grants-2000_11 |
|---|