Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N,N-dimethyl-1H-pyrazole-1-sulfonamide | HCID 10954038 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66743233 | HCID 66743233 | 68% |
Reaction Steps
To a stirred solution of N,N-dimethyl-1H-pyrazole-1-sulfonamide (25.3 g, 144 mmol) in THF (200 mL) at −78° C. was added dropwise 1.6 M n-butyllithium in hexane (99 ml, 159 mmol). After 30 min, iodoethane (12.8 mL, 159 mmol) was added dropwise. The reaction mixture was stirred at −78° C. for 30 min and allowed to room temperature slowly. After 1 h, the stirring became difficult by formation of white precipitate. THF (200 mL) was added dropwise to give yellow solution. The stirring was continued for 2 h. Then, the mixture was poured into saturated aqueous NaHCO3 (600 mL) and extracted with EtOAc (400 mL×2), and the extract was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (Purif, silica gel, hexane to 30:70 hexane/EtOAc) to afford the title compound (19.8 g, 68%) as colorless liquid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691828B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-cb9ca57a20fc4131afcbce8930b76f77 |
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| Source note | uspto-grants-2014_04 |
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