Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 70204259 | HCID 70204259 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70204323 | HCID 70204323 | 85.2% |
Reaction Steps
In 250 ml of absolute tetrahydrofuran, is dissolved 8.0 g (26.4 mmol) of trans-1-benzyloxycarbonyl-3-hydroxymethyl-4-trifluoromethylpyrrolidine. To the above solution, are added 4.27 g (29.0 mmol) of phthalimide and 8.30 g (31.7 mmol) of triphenylphosphine. Further, 5.0 ml (31.7 mmol) of azo dicarboxylic acid diethyl ester is added dropwise to the above solution on cooling with ice. After stirring at room temperature for 3 hours, the reaction mixture was concentrated under reduced pressure, and diethyl ether was added to the concentrated mixture to give a precipitate. The resulting precipitate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified with silica gel column chromatography (elusion solvent; chloroform/n-hexane (4/1→8/1)) to give 9.72 g of the objective substance as a colorless powder (yield 85.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668147 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-4da255477fc04024aec64f62cfed224b |
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| Source note | uspto-grants-1997_09 |
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