HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 6-((4-(4-cyano-5-(dicyanomethylene)-2-oxo-2,5-dihydro-1H-pyrrol-3-yl)phenyl)(2-ethylhexyl)amino)hexyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-((2-Ethylhexyl)(phenyl)amino)hexyl acetate | HCID 57857729 | — |
| Reactant | 4-Cyano-5-dicyanomethylene-3-hydroxy-2-oxo-3-pyrroline disodium salt | HCID 86634093 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-((4-(4-cyano-5-(dicyanomethylene)-2-oxo-2,5-dihydro-1H-pyrrol-3-yl)phenyl)(2-ethylhexyl)amino)hexyl acetate | HCID 86634094 | 38.8% |
Reaction Steps
In a three-neck flask, 6-((2-ethylhexyl)(phenyl)amino)hexyl acetate (7.0 g, 0.020 mol) was dissolved in dimethylformamide (100 ml), stirred, and added with acetic anhydride (2.9 g, 0.028 mol) and 4-cyano-5-dicyanomethylene-3-hydroxy-2-oxo-3-pyrroline disodium salt (5.6 g, 0.024 mol). The temperature was decreased to 0° C., after which POCl3 was slowly added thereto for 30 min, and the mixture was allowed to react at room temperature for 6 hours with stirring. A solid product was precipitated with water, filtered, and then dried, thus obtaining 4.0 g of a dark blue solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915428B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-70b8be560a674c16b274ff5c91c2b4c3 |
| Source note | uspto-grants-2011_03 |