HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522260Generated: October 29, 2026
Dimethylformamide → HCID 117913965, compound
https://huagongshe.com/reaction/522260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Benzyl-3-azabicyclo(3.2.1)octan-8-one | HCID 15639134 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 117913965 | HCID 117913965 | — |
Reaction Steps
60% sodium hydride (109 mg) was added to a mixture of triethyl phosphonoacetate (1.02 g) and THF (12 mL) at 0° C. in a nitrogen atmosphere, and the mixture was stirred at room temperature for 10 minutes. 3-Benzyl-3-azabicyclo[3.2.1]octan-8-one (978 mg) and DMF (5 mL) were added to the mixture, and the mixture was stirred at room temperature overnight. After water was added to the reaction mixture, extraction thereof was performed using EtOAc, and the extract was washed with saturated brine. The organic layer was dried over MgSO4 and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Hex:EtOAc=97:3 to 80:20), whereby ethyl(3-benzyl-3-azabicyclo[3.2.1]oct-8-ylidene)acetate (362 mg) was obtained as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328118B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8d621d2df33340ee93e2963a78559f42 |
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| Source note | uspto-grants-2016_05 |
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