Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | HCID 18429207 | HCID 18429207 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3,5-Dinitrostyrene | HCID 12192553 | — |
Reaction Steps
3,5-Dinitrophenylethanol (1.0 g, 4.7 mmol) was mixed with P2O5 (1.0 g, 0.71 mmol) and the stirred mixture was heated to 100° C. After 3 h, the mixture was allowed to cool to room temperature and water (0.4 ml) was added. The pH was adjusted to 9 using 1 M aqueous NaOH and extracted with diethyl ether (2×25 ml). The combined organic phases were dried (Na2SO4) and evaporated. The crude product was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310243B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-156b0e13f8d546adaa98d8109bc98fa6 |
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| Source note | uspto-grants-2001_10 |
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