Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,2-Benzenedicarboxylic acid, 4-nitro- | HCID 69121 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22457397 | HCID 22457397 | 136.7% |
Reaction Steps
4-nitrophthalic acid (2.0 g, 9.5 mmol) was dissolved in 30 ml of absolute ethanol and then 0.3 ml of concentrated sulfuric acid was added. The mixture was heated at 120° C. for 24 hours, and the solvent was evaporated under reduced pressure. The oily residue was dissolved in diethyl ether and washed three times with water and once with 10% Na2CO3 solution. The ether solution was dried over anhydrous sodium sulfate. After evaporation of the solvent, a light yellow crude solid was obtained. The crude product was purified by silica gel column chromatography (n-hexane: acetic acid =10:1) to give 2.1 g (68.4%) of di-n-butyl 4-nitrophthalate (compound 403).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399318B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-128edfc196634d60801854f711646ac2 |
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| Source note | uspto-grants-2002_06 |
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