Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 18770431 | HCID 18770431 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18770464 | HCID 18770464 | 61% |
Reaction Steps
Triethylamine (0.39 ml; 2.8 mmol), diphenylphosphoryl azide (0.61 ml; 2.8 mmol) and benzyl alcohol (0.39 ml; 3.8 mmol) were added to a solution in toluene (10 ml) of 2,2-bis[(1-tert-butoxycarbonyl-4-piperidinyl)methyl]acetic acid (850 mg; 1.9 mmol) synthesized by the above process, and the mixture was stirred for 12 hours in a bath controlled at 100° C. The reaction mixture was concentrated under reduced pressure, and the resultant concentrated residue was dissolved in ethyl acetate. This solution was washed successively with a saturated aqueous solution of sodium hydrogencarbonate and saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 639 mg (yield: 61%) of 2-benzyloxycarbonylamino-1,3-bis(1-tert-butoxycarbonyl-4-piperidinyl)propane as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448242B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-e5366b9c8c1e41f3a395f29b72abd8d7 |
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| Source note | uspto-grants-2002_09 |
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