HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25914Generated: October 27, 2026
2-(2',5'-Dimethoxybenzoyl)-6-methoxybenzoic acid → 1,4,5-Trimethoxyanthraquinone
https://huagongshe.com/reaction/25914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(2',5'-Dimethoxybenzoyl)-6-methoxybenzoic acid | HCID 13070649 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 1,4,5-Trimethoxyanthraquinone | HCID 12635716 | — |
Reaction Steps
2-(2',5'-Dimethoxybenzoyl)-6-methoxybenzoic acid (I) (3 g, 0.01 mole) was added in portions to stirred concentrated sulfuric acid (20 ml). After addition the mixture was heated on steam bath with constant stirring for 20 minutes, cooled to room temperature and poured onto crushed ice (400 g) and extracted with chloroform (3 × 100 ml). The organic extract was washed with 2% aqueous sodium hydroxide solution (10 × 100 ml) and water (100 ml), then dried over anhydrous sodium sulfate and the solvent stripped off under reduced pressure to yield 1,4,5-trimethoxyanthraquinone (II), as a brownish yellow solid (2.7 g, 90% yield). Recrystallization from ethanol gave yellow crystals, m.p. 201°-203° C.; IR (CDCl3), 5.92μ; NMR (CDCl3) δ, 7.88-7.20 (m, 5H), 3.94 (s, 3H), 3.92 (d, 6H). Calcd: C, 68.46; H, 4-70. Found: C, 68.33; H, 4.82.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04147706 |
|---|
| Source dataset | uspto-grants-1979_04 |
|---|
| ORD ID | ord-ccff36a1b32443578130857ec2e0f101 |
|---|
| Source note | uspto-grants-1979_04 |
|---|