Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-phenyl-2H-1-benzopyran | HCID 11063647 | — |
| Solvent | Dichloromethane cyclohexane | HCID 21916607 | — |
| Product | HCID 18185263 | HCID 18185263 | 83% |
Reaction Steps
71 ml (0.773 mol) of phosphorus oxychloride are added dropwise to 300 ml of dimethylformamide maintained at 0° C. The reaction mixture is left stirring for 20 minutes at a temperature of between 0 and 5° C. A solution of 16.1 g (77.3 mmol) of 4-phenyl-2H-1-benzopyran in 22.5 ml of dimethylformamide is then added to the reaction mixture. The reaction mixture is allowed to return to room temperature and is then brought to 60° C. for 7 hours. The reaction mixture is then poured into a mixture of ice and water which is neutralized with NaOH. The organic phase is extracted with ethyl acetate and then the organic phase is washed 3 times with water. After drying over anhydrous sodium sulphate, the organic phase is concentrated under reduced pressure. A pasty solid is thus obtained, which solid, after silica column chromatography using a 1/1 methylene chloride/cyclohexane mixture as eluant, results in 15.3 g of the title compound in the form of a yellow solid, the melting point of which is 82-83° C. (yield=83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06596758B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-7cef4b7fa45044ac99ab173765f6b2da |
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| Source note | uspto-grants-2003_07 |
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