Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | bismuth(III) bromide | HCID 82232 | — |
| Reactant | HCID 178455354 | HCID 178455354 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178468173 | HCID 178468173 | 42.7% |
Reaction Steps
Acetaldehyde (10 mL; 0.17 mol) in acetonitrile (50 mL) was added over 30 minutes to a solution of trans-N-(4-tert-butyldimethylsilyloxycyclohexyl)phthalimide (D63; 50.0 g; 0.14 mol), bismuth tribromide (6.7 g; 0.015 mol) and triethylsilane (27 mL; 0.18 mol) in acetonitrile (500 mL) stirred at ice bath temperature and the mixture was allowed to warm to room temperature overnight. The mixture was filtered and the resulting grey solid and filtrate were worked up separately. The filtrate was evaporated and treated with hexane to give the title compound as a white solid (16.35 g). The grey solid was washed with dichloromethane, the dichloromethane extract was evaporated and the residue was stirred with hexane (200 mL) to give a second crop of the title compound as a white solid (17.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278328B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-3c3a7d8bdca0421cbdb6dd9fcd1ba788 |
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| Source note | uspto-grants-2012_10 |
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