Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Palmitoyl chloride | HCID 8206 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 70558552 | HCID 70558552 | — |
| Product | HCID 68176657 | HCID 68176657 | — |
Reaction Steps
5,7-Dihydroxymethylchromone (15 g, 78 mmol) is dissolved in N,N-dimethylformamide (360 ml), and potassium tert-butoxide (9 g, 80 mmol) is added to the brown solution under a stream of nitrogen. The mixture is subsequently heated at 30° C. for 2.5 h. Palmitoyl chloride (24 ml, 79.5 mmol) in N,N-dimethylformamide (80 ml) is then slowly added dropwise to the solution at 30° C. The resultant suspension is stirred at 30° C. for a further 2 hours, and 400 ml of DI water are then added dropwise. After 1 hour, the solid is filtered off with suction via a suction filter, dried well by suction and dried at 40° C. in a vacuum drying cabinet.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382224B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-57f8f9873bae477cb573aea59de70f82 |
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| Source note | uspto-grants-2016_07 |
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