HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900390Generated: October 25, 2026
4-t-Butyl-2-(4-t-butylbenzoyl)benzoic acid → 2,7-Di-t-butylanthraquinone
https://huagongshe.com/reaction/900390
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-t-Butyl-2-(4-t-butylbenzoyl)benzoic acid | HCID 7730272 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,7-Di-t-butylanthraquinone | HCID 357626 | 69% |
Reaction Steps
Into a 500 ml flask having the egg plant shape equipped with a condenser, 200 ml of polyphosphoric acid was placed and heated at 150° C. Then, 32 g (95 mmole) of 4-t-butyl-2-(4-t-butylbenzoyl)benzoic acid was added in small portions, and the resultant mixture was stirred at the same temperature for 3 hours. After the reaction was completed, the reaction mixture was poured into ice water, and the resultant mixture was treated by liquid-liquid extraction with chloroform. After being dried with magnesium sulfate, the extract was concentrated under a reduced pressure by a rotary evaporator. The obtained crude crystals were recrystallized from hexane, and 21 g of the anthraquinone compound of the object compound was obtained (the yield: 69%; yellow crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07357991B2 |
|---|
| Source dataset | uspto-grants-2008_04 |
|---|
| ORD ID | ord-7a09d4afdd9146cdae94a331d3449c85 |
|---|
| Source note | uspto-grants-2008_04 |
|---|