Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 54329089 | HCID 54329089 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 17967911 | HCID 17967911 | 82.1% |
Reaction Steps
A mixture of 1-(4-benzyloxy-benzenesulfonyl)-5-hydroxy-5-methyl-piperidine-2-carboxylic acid methyl ester (0.047 g, 0.11 mmol), p-toluenesulfonic acid (0.010 g, 0.05 mmol) and toluene (2.0 mL) was heated to 90° C. for 2 h. After cooling to room temperature, the mixture was diluted with ethyl acetate, washed with saturated aqueous NaHCO3, dried over Na2SO4, filtered and concentrated in vacuo, giving 0.035 g of 5-(4-Benzyloxy-benzenesulfonyl)-1-methyl-2-oxa-5-aza-bicyclo[2.2.2]octan-3-one as a colorless oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329397B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-35e005c2734e4a35b298b05a5af2c449 |
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| Source note | uspto-grants-2001_12 |
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