Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Reactant | HCID 15297474 | HCID 15297474 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Phthalonitrile | HCID 7042 | 131% |
Reaction Steps
In 180 ml of N,N-dimethylformamide were dissolved with heating 20 g of 3-hydroxyphthalonitrile and 10.55 g of potassium carbonate, to which 18 g of chloromethyltrimethyl-silane were added dropwise at 40° C. in the atmosphere of argon. After the addition, the mixture was stirred for 30 hours while maintaining the reaction temperature at 80°-90° C. The reaction vessel was then cooled to room temperature and 250 ml of dilute hydrochloric acid was added. The mixture was extracted with 1.2 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 23.3 g (yield: 73.0%) of a compound having the formula (XII) below. The compound is in the form of white crystals and has a melting point of 112.5° C. The IR spectrum of the compound is shown in FIG. 3. ##STR37##
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-58d4871eba9a46168c4e5d179f46ce31 |
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| Source note | uspto-grants-1997_10 |
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