Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Tert-butyl 4-cyano-4-(dimethylamino)piperidine-1-carboxylate | HCID 57504797 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 57831240 | HCID 57831240 | 64.1% |
Reaction Steps
To a mixture of 5.6 g (3 equiv.) of magnesium and 20 ml of dry diethyl ether there were added first a small amount of iodine and then, over a period of 10 minutes, 5 g of 2-bromothiophene, and stirring was carried out for a further 10 minutes. When the reaction had started, 33.5 g (2.6 equiv.) of 2-bromothiophene dissolved in 80 ml of diethyl ether were added dropwise, and stirring was carried out over a period of 2 hours at room temperature. The Grignard reagent prepared above was added dropwise to a solution of 20 g (1 equiv.) of tert-butyloxycarbonyl-4-cyano-4-(dimethylamino)piperidine dissolved in 200 ml of THF, and stirring was carried out overnight at room temperature. The progress of the reaction was monitored by thin-layer chromatography (50% EtOAc/hexane). When the reaction was complete, the reaction solution was cooled to 0° C., saturated NH4Cl solution was added, extraction with ethyl acetate (3×100 ml) was carried out, and the combined organic phases were dried with Na2SO4. After removal of the solvent under reduced pressure, purification was carried out by column chromatography (Alox Neutral; 30% EtOAc/hexane). 6.1 g (25%) of product were obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08269000B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-452a11b590b04cb8ae2b5d5ea5f51dcc |
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| Source note | uspto-grants-2012_09 |
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