Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | HCID 86609417 | HCID 86609417 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68766704 | HCID 68766704 | 33.1% |
Reaction Steps
To a solution of (E)-4-(t-butyldimethylsilyloxy)-3-(formylmethylidene)-1-(triphenylmethyl)piperidine (112 mg) in methanol (2.5 ml) were added successively p-toluenesulfonylmethyl isocyanide (45 mg) and potassium carbonate (32 mg), and the resulting mixture was refluxed for 3.5 hours. After refluxing, water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution, and the organic layer was dried over anhydrous sodium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:19 to 1:3) as the eluent to afford the title compound (40 mg, yield: 32%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829580B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-d42228b524304af58aba019f0404eee1 |
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| Source note | uspto-grants-2010_11 |
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