HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fuming sulfuric acid → Acenaphtho[1,2-b]quinoxaline-2,5-disulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fuming sulfuric acid | HCID 24681 | — |
| Reactant | Acenaphtho[1,2-b]quinoxaline | HCID 136028 | — |
| Solvent | Water | HCID 962 | — |
| Product | Acenaphtho[1,2-b]quinoxaline-2,5-disulfonic acid | HCID 22141822 | — |
Reaction Steps
Acenaphtho[1,2-b]quinoxaline (10 g) was charged into 10% oleum (49 ml), stirredfor 30 minutes and heated at 180–190° C. for 30 hours. The reaction mixture was then diluted with water (95 ml), and the formed precipitate was filtered and washed with acetic acid (˜30 ml). The filtered cake was dried on air at 120° C. to yield 8.2 g of acenaphtho[1,2-b]quinoxaline-2,5-disulfonic acid. 1H NMR (Bruker AMX-400, DMSO-d6, δ, ppm): 7.82 (q, 2H, 3 Hz); 8.18 (q, 2H, 3 Hz); 8.24–8.36 (broad s, 2H); 8.62 (s, 4H). Elemental analysis calculated for C18H10N2O6S2: C, 52.17; H, 2.43; N, 6.76; found: C, 52.02; H, 2.35; N, 6.56.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07045177B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-ad85bda286234de88ea0a1b83f1ea4c1 |
| Source note | uspto-grants-2006_05 |