Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 68971662 | HCID 68971662 | — |
| Product | HCID 68970622 | HCID 68970622 | 61% |
Reaction Steps
To solution of the above sulfide (1.2 g, 3.58 mmol) in MeOH (58 mL) cooled to 0° C. was added OXONE® (4.40 g, 7.15 mmol) and the mixture was stirred at 0° C. for 4 hours to afford 4-(4-methanesulfonyl-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester as a white solid (802 mg, 61%) after basic work-up and purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07491735B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-a60ac923bced44b6a73007c7a0f01603 |
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| Source note | uspto-grants-2009_02 |
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