Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | HCID 9921425 | HCID 9921425 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Catalyst | Ruthenium trichloride | HCID 61850 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 9813358 | HCID 9813358 | 14% |
Reaction Steps
((1S,3R)-1-Benzyl-3-methyl-cyclopentylmethyl)-carbamic acid methyl ester (2.6 g, 9.9 mmol) and sodium periodate (29.8 g, 140 mmol) were stirred together in carbon tetrachloride (30 mL), acetonitrile (30 mL), and water for 6 hours. The mixture was cooled to 0° C., and ruthenium(III) chloride (0.04 g, 0.2 mmol) was added to the reaction mixture. The reaction was allowed to warm to room temperature and stirred for 20 hours. Diethyl ether (50 mL) was added, and the mixture was then extracted with saturated aqueous sodium hydrogen carbonate (200 mL). The aqueous layer was acidified to pH 1 with 4N hydrochloric acid and re-extracted with ethyl acetate (200 mL), dried (MgSO4), and the solvent was evaporated under reduced pressure. The residue was purified by chromatography (silica gel, eluting with a gradient of heptane to 1:1 heptane:ethyl acetate) to give 0.32 g (14%) of [(1S,3R)-1-(methoxycarbonylamino-methyl)-3-methyl-cyclopentyl]-acetic acid;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06864390B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-7043762af2f84d83bfd7cdaa2e1144a8 |
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| Source note | uspto-grants-2005_03 |
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