Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178419313 | HCID 178419313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 67260464 | HCID 67260464 | 7% |
| Product | HCID 67260594 | HCID 67260594 | 81% |
Reaction Steps
3-(4,5-dibromo-2-thienyl)-1H-pyrazole (9.4 mmol) was dissolved in 20 mL dry N,N-dimethylformamide under argon atmosphere. Sodium hydride (11.3 mmol, 60% dispersion in mineral oil) was added in portions at room temperature. The reaction mixture was stirred at room temperature for 15 min. Isopropyl iodide (14.1 mmol) was added dropwise and the reaction mixture was stirred at room temperature for 14 h. Water and MTBE were added to the reaction mixture. The phases were separated and the aqueous phase was extracted with MTBE. The combined organic extracts were successively washed with water and brine, dried over MgSO4, filtered and concentrated. The residue was purified by chromatography on silica gel (toluene:ethyl acetate 100:0 to 0:100) to afford 2.67 g 3-(4,5-dibromo-2-thienyl)-1-isopropyl-1H-pyrazole (81% yield) and 238 mg of 5-(4,5-dibromo-2-thienyl)-1-isopropyl-1H-pyrazole (7% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08685974B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-9cbfe29a60d34327b26ca32db2feffba |
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| Source note | uspto-grants-2014_04 |
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