Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenepropanal | HCID 7707 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 9834042 | HCID 9834042 | 99.2% |
Reaction Steps
Vinylmagnesium Bromide (120 mmol, 1M) in ether was added to 80 ml of dry tetrahydrofuran and cooled under inert atmosphere to 0° C. Hydrocinnamaldehyde (8.0 ml, 61 mmol) was added dropwise, and the solution was stirred for 10 min, quenched cautiously with saturated aqueous ammonium chloride, extracted with ether, washed with saturated brine, dried over MgSO4, and concentrated to give 9.82 g (98.6%) of the crude desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05142056 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-50d6decde34043188d932efd9bca1a71 |
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| Source note | uspto-grants-1992_08 |
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