Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium periodate | HCID 23667635 | — |
| Reactant | HCID 178483639 | HCID 178483639 | — |
| Catalyst | Ruthenium trichloride | HCID 61850 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 178483642 | HCID 178483642 | 62.4% |
Reaction Steps
0.66 g (2.3 mmol) of trans-methyl-{2-[4-(2-oxo-ethyl)-cyclohexyl]-ethyl}-carbamic acid tert-butyl ester were dissolved in 2 mL of CCl4, 2 mL of acetonitrile and 3 mL of water. To this mixture were added 2.4 mg (0.012 mmol, 0.01 eq) of anhydrous ruthenium (III) chloride, followed by 2.04 g (9.5 mmol, 4.1 eq) of sodium metaperiodate in small portions. Stirring was continued at RT for 2 h, the mixture was filtered and partitioned between CH2Cl2 and water. The organic phase was washed with water and dried over magnesium sulfate. Column chromatography of the crude product with a gradient of n-heptane: EtOAc 1:4 to 1:1 gave 430 mg (62%) of trans-{4-[2-(tert-butoxycarbonyl-methyl-amino)-ethyl]-cyclohexyl}-acetic acid as colorless oil, MS: 317 (M+NH4+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06965048B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-50e2c9eec1604330827a0fe23716df92 |
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| Source note | uspto-grants-2005_11 |
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