Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Furancarbonyl chloride | HCID 68242 | — |
| Reactant | N,N-Dimethylpropargylamine | HCID 81643 | — |
| Product | HCID 565761 | HCID 565761 | — |
Reaction Steps
2-Furoyl chloride (6.5 gm, 0.05 m) was dissolved in methylene chloride- (200 ml), cooled to 0° to -5° C. and maintained under a nitrogen atmosphere. Triethylamine (10 ml) and then dimethylpropargylamine (4.2 gm, 0.051 m) were gradually added with stirring while maintaining the temperature at 0°±5° C. for about one-half hour and then at room temperature for about 1 hour. Water .(100 ml) was added and the reaction slurry was transferred, using methylene chloride (100 ml ) as a rinse, to a separatory funnel. The aqueous layer was sequentially separated and the methylene chloride layer was washed with water (50 ml ), 5% hydrochloric acid (1×100 ml ), saturated sodium bicarbonate (1×50 ml), water (1×50 ml) and then brine. The solvent was evaporated after drying over magnesium sulfate and 8.0 gms of product were obtained. The starting materials for all compounds except 7, 8 and 11 can be prepared in an analogous manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344978 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-021cf0f8f1d940f6852932f54a043ce9 |
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| Source note | uspto-grants-1994_09 |
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