Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 3,3-Dimethylbutanal | HCID 76335 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | tert-Butyl (2R)-2-(aminomethyl)piperidine-1-carboxylate | HCID 1502021 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66661021 | HCID 66661021 | — |
Reaction Steps
To a solution of 3,3-dimethylbutanal (439 mg, 4.39 mmol) in acetonitrile (8 mL) was added molecular sieves (4A beads, 8-12 mesh, 0.7 g) and (R)-tert-butyl 2-(aminomethyl)piperidine-1-carboxylate (940 mg, 4.39 mmol). The mixture was stirred for 12 hr at room temperature, filtered and washed with acetonitrile (5 mL). To this solution was added potassium thiocyanate (567 mg, 5.83 mmol) and the temperature was adjusted at 50° C. The reaction was stirred until all solids were dissolved then iodine (1.13 g, 4.39 mmol) was added. The reaction was stirred at 50° C. for 12 hr. The mixture was then stirred with 20% sodium metabisulfite for 1 hr. Then the organic layer was separated and the aqueous layer was extracted with dichloromethane (3×10 mL). The combined organics were dried over sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. This intermediate was used without further purification. MS (DCI/NH3) m/z 354 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875640B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-ea96668e1d814ba2806cd30fefeee67b |
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| Source note | uspto-grants-2011_01 |
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