Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Reactant | 1,2-Benzenedicarbonitrile, 3-nitro- | HCID 162652 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | N,N-dimethylacetamide 1-methyl-2-pyrrolidone | HCID 22717425 | — |
| Product | Phthalonitrile | HCID 7042 | 134.2% |
Reaction Steps
In 180 ml of an N,N-dimethylacetamide/1-methyl-2-pyrrolidone (=1/1 volume ratio) mixed solvent were dissolved 30 g of 3-nitrophthalonitrile, to which 11.97 g of sodium nitrite were added. The mixture was stirred at 165° C. for 40 minutes. After being cooled to room temperature, the mixture was added with 16.8 g of potassium carbonate, which was further stirred at 150° C. for 40 minutes and thereafter cooled to 40° C. Then, 25 g of chloromethyltrimethylsilane were added dropwise. After the addition, the mixture was stirred for 28 hours while maintaining the reaction temperature at 80°-90° C. The reaction vessel was then cooled to room temperature and 350 ml of dilute hydrochloric acid was added. The mixture was extracted with 1.5 liters of toluene. The organic layer was washed well with water and water was removed with magnesium sulfate. Thereafter, toluene was removed by distillation and the residue was purified with a toluene/silica gel column to obtain 29.8 g (yield: 74.7%) of a compound having the above-described formula (XV).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677025 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-ead03d4903234b6a860ceaeb23f2100b |
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| Source note | uspto-grants-1997_10 |
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