HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → Anthraquinone-2-carbonyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Anthraquinonecarboxylic acid | HCID 67030 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Anthraquinone-2-carbonyl Chloride | HCID 15025286 | — |
Reaction Steps
The compound of Structure (I-C) was prepared as follows. 2-carboxyanthraquinone was reacted with oxalyl chloride in dichloromethane (catalyzed by dimethylformamide) to yield 2-chlorocarbonylanthraquinone, which was then reacted with 1-hexanol in tetrahydrofuran (in the presence of triethylamine) to yield 2-n-hexoxycarbonylanthraquinone, which was then treated in a manner similar to Preparation A to prepare the Structure (I-C) compound with a yield of 50%. Structure was confirmed by IR and NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04913996 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-1aade12be2404a799099d9c145ff8cb2 |
| Source note | uspto-grants-1990_04 |