Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylpyridine | HCID 7963 | — |
| Reactant | Ethyl 5-chlorothiophene-2-carboxylate | HCID 521808 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 65583291 | HCID 65583291 | — |
Reaction Steps
At 0° C., 64.5 ml of a 1M solution of lithium bis(trimethylsilyl)amide in hexane are added dropwise to a solution of 3.00 g (32.3 mmol) of 4-methylpyridine and 6.77 g (35.5 mmol) of ethyl 5-chlorothiophene-2-carboxylate in 58 ml THF, and the reaction mixture is stirred at 5° C. for 3 h. The resulting precipitate was filtered off, acidified with 6M HCl, filtered again and dried. This gives 2.9 g (35%) of the desired product; 1H-NMR (DMSO-d6): δ=8.53 (d, 2H), 8.09 (d, 1H), 7.40 (d, 1H), 7.34 (d, 2H), 4.39 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09198426B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-2559aebc93ea47b19234463dba5e3caa |
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| Source note | uspto-grants-2015_12 |
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