HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234247Generated: October 26, 2026
Sodium Bicarbonate → 5,12-Naphthacenedione, 1,2,3,4-tetrahydro-
https://huagongshe.com/reaction/234247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ammonium cerium-nitrate | HCID 57418452 | — |
| Reactant | Octahydro-11-naphthacenone | HCID 67719023 | — |
| Catalyst | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5,12-Naphthacenedione, 1,2,3,4-tetrahydro- | HCID 621483 | 147.4% |
Reaction Steps
A solution of 36 mg (0.075 mmol) of the octahydro-11-naphthacenone and 60 mg (0.675 mmol) of NaHCO3 in 10 mL of acetone was treated with a solution of 167 mg (3 mmol) of cerium ammonium nitrate (CAN) and 1 mg of dichlorodicyanobenzoquinone (DDQ) in 2 mL of acetone added in one portion at 0 degrees centigrade. The reaction mixture was stirred at room temperature for 1.5 hours during which the color changed from shiny yellow to orange red, and then 25 mL of CH2Cl2 was added. The mixture was filtered through over Celite. The organic layer was washed with saturated NaCl solution (2×20 mL), dried over Na2SO4, and evaporated to give the tetrahydro-5,12-naphthacenedione as a red crystals (29 mg, 86 percent). mp greater than 258 degrees centigrade (decomp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594158 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-f13e9e299b6c42f3a7fac25c2d29c638 |
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| Source note | uspto-grants-1997_01 |
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