HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274512Generated: October 30, 2026
Ethanol → Ethyl(3,4-dihydroxy-5-nitrobenzoyl)acetate
https://huagongshe.com/reaction/274512
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Diethyl 3,4-dimethoxy-5-nitrobenzoylmalonate | HCID 19000155 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl(3,4-dihydroxy-5-nitrobenzoyl)acetate | HCID 21459116 | — |
Reaction Steps
20.1 g of diethyl (3,4-dimethoxy-5-nitrobenzoyl)-malonate are dissolved in 200 ml of methylene chloride, whereupon the solution is cooled to -20° and at this temperature there is added dropwise while stirring within 15 minutes a solution of 68.1 g of boron tribromide in 120 ml of methylene chloride. The mixture is subsequently stirred at room temperature overnight. After cooling to -20° , the mixture is treated with 300 ml of ethanol and stirred at room temperature for 30 minutes. The solvent is distilled in a water-jet vacuum at 40° . The residue is treated with 300 ml of ice-water and methylene chloride. The organic phase is washed with water, dried over sodium sulfate and evaporated. The crude product obtained is chromatographed on a 10-fold amount of silica gel with toluene. After crystallization from methylene chloride/hexane there is obtained ethyl (3,4-dihydroxy-5-nitrobenzoyl)acetate in the form of yellow crystals of m.p. 136°-137°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389653 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-f4c4085356fe4424b02fec0fd474e987 |
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| Source note | uspto-grants-1995_02 |
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