Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methanesulfonic acid 1-methoxy-piperidin-4-yl ester | HCID 86663299 | — |
| Catalyst | Tetrabutylammonium Cyanide | HCID 165872 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-Methoxypiperidine-4-carbonitrile | HCID 66793970 | 86.6% |
Reaction Steps
200 mg Methanesulfonic acid 1-methoxy-piperidin-4-yl ester (from Step 2), 251 mg tetrabutylammonium cyanide and 272 mg sodium cyanide were mixed in 1 ml dimethylsulfoxide, and heated to 55° C. for 18 hours. Then the mixture was cooled to room temperature, 1 ml saturated aqueous sodium bicarbonate and 3 ml water were added, and extracted three times with diethyl ether. The organic layer was dried over anhydrous sodium sulfate and the solvent evaporated. The residue was purified by chromatography on silica gel with ethyl acetate/cyclohexane (1:1, then 2:1, then pure ethyl acetate) as a solvent. 116 mg 1-methoxy-piperidine-4-carbonitrile was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08574607B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-979cb16aaf744ea7aa02586e523dc5eb |
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| Source note | uspto-grants-2013_11 |
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